{
  "snapshot_date": "2026-08-21",
  "product_code": "OAP",
  "field_notes": {
    "applicant": "The entity that filed the 510(k), not necessarily the consumer brand.",
    "fda_record_url": "The FDA record for the published clearance number.",
    "omitted_columns": "state and country_code are omitted for every row because the report measures findability, not geography."
  },
  "rows": [
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Lexington International, LLC",
      "clearance_type": "Traditional",
      "date_received": "2006-02-06",
      "decision_code": "SESE",
      "decision_date": "2007-01-18",
      "decision_description": "Substantially Equivalent",
      "device_name": "HAIRMAX LASERCOMB",
      "k_number": "K060305",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K060305"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Lexington International, LLC",
      "clearance_type": "Special",
      "date_received": "2009-11-12",
      "decision_code": "SESE",
      "decision_date": "2009-11-23",
      "decision_description": "Substantially Equivalent",
      "device_name": "HAIRMAX LASERCOMB",
      "k_number": "K093499",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K093499"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Midwest Rf, LLC",
      "clearance_type": "Traditional",
      "date_received": "2009-05-20",
      "decision_code": "SESE",
      "decision_date": "2010-02-23",
      "decision_description": "Substantially Equivalent",
      "device_name": "MEP-90 HAIR GROWTH STIMULATION SYSTEM",
      "k_number": "K091496",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K091496"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Lexington International, LLC",
      "clearance_type": "Traditional",
      "date_received": "2010-11-17",
      "decision_code": "SESE",
      "decision_date": "2011-04-06",
      "decision_description": "Substantially Equivalent",
      "device_name": "HAIRMAX LASERCOMB",
      "k_number": "K103368",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K103368"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Lexington International, LLC",
      "clearance_type": "Traditional",
      "date_received": "2011-01-26",
      "decision_code": "SESE",
      "decision_date": "2011-05-27",
      "decision_description": "Substantially Equivalent",
      "device_name": "HAIRMAX LASERCOMB",
      "k_number": "K110233",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K110233"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Lexington International, LLC",
      "clearance_type": "Traditional",
      "date_received": "2011-06-20",
      "decision_code": "SESE",
      "decision_date": "2011-08-16",
      "decision_description": "Substantially Equivalent",
      "device_name": "HAIRMAX DUAL 12",
      "k_number": "K111714",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K111714"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Lexington International, LLC",
      "clearance_type": "Special",
      "date_received": "2011-08-31",
      "decision_code": "SESE",
      "decision_date": "2011-09-26",
      "decision_description": "Substantially Equivalent",
      "device_name": "HAIRMAX LASERCOMB",
      "k_number": "K112524",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K112524"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Theradome, Inc.",
      "clearance_type": "Traditional",
      "date_received": "2011-10-19",
      "decision_code": "SESE",
      "decision_date": "2012-03-02",
      "decision_description": "Substantially Equivalent",
      "device_name": "LASER HELMET",
      "k_number": "K113097",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K113097"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Apira Science, Inc.",
      "clearance_type": "Traditional",
      "date_received": "2012-07-27",
      "decision_code": "SESE",
      "decision_date": "2012-12-05",
      "decision_description": "Substantially Equivalent",
      "device_name": "IGROW II HAIR GROWTH SYSTEM",
      "k_number": "K122248",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K122248"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Theradome, Inc.",
      "clearance_type": "Traditional",
      "date_received": "2012-09-25",
      "decision_code": "SESE",
      "decision_date": "2013-06-14",
      "decision_description": "Substantially Equivalent",
      "device_name": "LASER HELMET",
      "k_number": "K122950",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K122950"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Sunetics International Marketing Group, LLC",
      "clearance_type": "Traditional",
      "date_received": "2012-07-02",
      "decision_code": "SESE",
      "decision_date": "2013-06-27",
      "decision_description": "Substantially Equivalent",
      "device_name": "LASERBRUSH",
      "k_number": "K121920",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K121920"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Sunetics International Marketing Group, LLC",
      "clearance_type": "Traditional",
      "date_received": "2013-08-26",
      "decision_code": "SESE",
      "decision_date": "2013-12-20",
      "decision_description": "Substantially Equivalent",
      "device_name": "SUNETICS CLINICAL BIO-STIMULATION LASER",
      "k_number": "K132646",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K132646"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Apira Science, Inc.",
      "clearance_type": "Traditional",
      "date_received": "2014-06-12",
      "decision_code": "SESE",
      "decision_date": "2014-08-21",
      "decision_description": "Substantially Equivalent",
      "device_name": "IGROW - II HAIR GROWTH SYSTEM, IGROW HAIR GROWTH SYSTEM",
      "k_number": "K141567",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K141567"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Lexington International, LLC",
      "clearance_type": "Traditional",
      "date_received": "2014-09-12",
      "decision_code": "SESE",
      "decision_date": "2014-12-01",
      "decision_description": "Substantially Equivalent",
      "device_name": "HairMax LaserComb, HairMax LaserComb",
      "k_number": "K142573",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K142573"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Apira Science, Inc.",
      "clearance_type": "Traditional",
      "date_received": "2014-04-11",
      "decision_code": "SESE",
      "decision_date": "2014-12-05",
      "decision_description": "Substantially Equivalent",
      "device_name": "IGROW II HAIR GROWTH SYSTEM",
      "k_number": "K140931",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K140931"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Nutra Luxe MD, LLC",
      "clearance_type": "Traditional",
      "date_received": "2014-06-13",
      "decision_code": "SESE",
      "decision_date": "2015-01-08",
      "decision_description": "Substantially Equivalent",
      "device_name": "NUTRA STIM HAIR LASER COMB",
      "k_number": "K141588",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K141588"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Nutra Luxe MD, LLC",
      "clearance_type": "Traditional",
      "date_received": "2014-06-13",
      "decision_code": "SESE",
      "decision_date": "2015-01-08",
      "decision_description": "Substantially Equivalent",
      "device_name": "NUTRA STIM HAIR LASER COMB",
      "k_number": "K141596",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K141596"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Capillus, LLC",
      "clearance_type": "Traditional",
      "date_received": "2014-11-06",
      "decision_code": "SESE",
      "decision_date": "2015-01-29",
      "decision_description": "Substantially Equivalent",
      "device_name": "Capillus 272 Pro",
      "k_number": "K143199",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K143199"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Hairlabs International, Inc.",
      "clearance_type": "Traditional",
      "date_received": "2014-09-30",
      "decision_code": "SESE",
      "decision_date": "2015-04-14",
      "decision_description": "Substantially Equivalent",
      "device_name": "LX-100 Hair Growth Stimulation System",
      "k_number": "K142824",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K142824"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Capillus, LLC",
      "clearance_type": "Traditional",
      "date_received": "2015-03-09",
      "decision_code": "SESE",
      "decision_date": "2015-06-09",
      "decision_description": "Substantially Equivalent",
      "device_name": "Capillus 272 Office Pro",
      "k_number": "K150578",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K150578"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Transdermal Cap, Inc.",
      "clearance_type": "Traditional",
      "date_received": "2015-03-10",
      "decision_code": "SESE",
      "decision_date": "2015-07-22",
      "decision_description": "Substantially Equivalent",
      "device_name": "LaserCap LC Pro and LC Elite",
      "k_number": "K150613",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K150613"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Capillus, LLC",
      "clearance_type": "Special",
      "date_received": "2015-06-05",
      "decision_code": "SESE",
      "decision_date": "2015-08-21",
      "decision_description": "Substantially Equivalent",
      "device_name": "Capillus82",
      "k_number": "K151516",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K151516"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Trophy Skin, Inc.",
      "clearance_type": "Traditional",
      "date_received": "2015-07-21",
      "decision_code": "SESE",
      "decision_date": "2015-11-16",
      "decision_description": "Substantially Equivalent",
      "device_name": "HairMD",
      "k_number": "K152019",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K152019"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Freedom Laser Therapy, Inc.",
      "clearance_type": "Traditional",
      "date_received": "2015-06-19",
      "decision_code": "SESE",
      "decision_date": "2016-01-06",
      "decision_description": "Substantially Equivalent",
      "device_name": "iRestore",
      "k_number": "K151662",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K151662"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Capillus, LLC",
      "clearance_type": "Special",
      "date_received": "2015-12-18",
      "decision_code": "SESE",
      "decision_date": "2016-01-19",
      "decision_description": "Substantially Equivalent",
      "device_name": "Capillus202",
      "k_number": "K153618",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K153618"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Dermascalp, LLC",
      "clearance_type": "Traditional",
      "date_received": "2015-09-10",
      "decision_code": "SESE",
      "decision_date": "2016-02-04",
      "decision_description": "Substantially Equivalent",
      "device_name": "DermaScalp Laser Cap",
      "k_number": "K152587",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K152587"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Capillus, LLC",
      "clearance_type": "Traditional",
      "date_received": "2016-02-03",
      "decision_code": "SESE",
      "decision_date": "2016-04-25",
      "decision_description": "Substantially Equivalent",
      "device_name": "Capillus272 Pro, Capillus272 OfficePro, Capillus82, Capillus202",
      "k_number": "K160285",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K160285"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Theradome, Inc.",
      "clearance_type": "Special",
      "date_received": "2016-04-13",
      "decision_code": "SESE",
      "decision_date": "2016-05-12",
      "decision_description": "Substantially Equivalent",
      "device_name": "Laser Helmet LH40-EVO",
      "k_number": "K161046",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K161046"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Nutra Luxe MD, LLC",
      "clearance_type": "Traditional",
      "date_received": "2016-03-16",
      "decision_code": "SESE",
      "decision_date": "2016-09-16",
      "decision_description": "Substantially Equivalent",
      "device_name": "NutraStim Hair Laser Helmet",
      "k_number": "K160728",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K160728"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Transdermal Cap, Inc.",
      "clearance_type": "Traditional",
      "date_received": "2016-07-08",
      "decision_code": "SESE",
      "decision_date": "2016-09-30",
      "decision_description": "Substantially Equivalent",
      "device_name": "LaserCap300, LaserCap224, LaserCap120, LaserCap80",
      "k_number": "K161875",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K161875"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Capillus, LLC",
      "clearance_type": "Special",
      "date_received": "2016-10-27",
      "decision_code": "SESE",
      "decision_date": "2016-11-18",
      "decision_description": "Substantially Equivalent",
      "device_name": "Capillus302, Capillus312, Capillus352",
      "k_number": "K162994",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K162994"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Capillus, LLC",
      "clearance_type": "Traditional",
      "date_received": "2016-11-14",
      "decision_code": "SESE",
      "decision_date": "2017-01-31",
      "decision_description": "Substantially Equivalent",
      "device_name": "Capillus 82, Capillus 202, Capillus 272 Pro, 272 Office Pro, Capillus 302, Capillus 312, and Capillus 352",
      "k_number": "K163170",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K163170"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Eglobal, LLC",
      "clearance_type": "Traditional",
      "date_received": "2016-07-27",
      "decision_code": "SESE",
      "decision_date": "2017-02-24",
      "decision_description": "Substantially Equivalent",
      "device_name": "IllumiFlow Laser Cap",
      "k_number": "K162071",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K162071"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Slinph Technologies Co., Ltd.",
      "clearance_type": "Traditional",
      "date_received": "2016-10-03",
      "decision_code": "SESE",
      "decision_date": "2017-04-04",
      "decision_description": "Substantially Equivalent",
      "device_name": "iHelmet Hair Growth System",
      "k_number": "K162782",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K162782"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Leana Orders, Inc.",
      "clearance_type": "Traditional",
      "date_received": "2017-06-26",
      "decision_code": "SESE",
      "decision_date": "2017-08-22",
      "decision_description": "Substantially Equivalent",
      "device_name": "Grivamax Hair Growth System",
      "k_number": "K171895",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K171895"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Super Grow Lasers",
      "clearance_type": "Traditional",
      "date_received": "2017-09-27",
      "decision_code": "SESE",
      "decision_date": "2017-12-19",
      "decision_description": "Substantially Equivalent",
      "device_name": "SuperGrow 272, Ultimate 272",
      "k_number": "K172982",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K172982"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Y & J Bio Co., Ltd.",
      "clearance_type": "Traditional",
      "date_received": "2017-09-26",
      "decision_code": "SESE",
      "decision_date": "2018-01-05",
      "decision_description": "Substantially Equivalent",
      "device_name": "Hair Up",
      "k_number": "K172968",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K172968"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Theradome, Inc.",
      "clearance_type": "Traditional",
      "date_received": "2017-06-14",
      "decision_code": "SESE",
      "decision_date": "2018-01-09",
      "decision_description": "Substantially Equivalent",
      "device_name": "Theradome LH80 PRO",
      "k_number": "K171775",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K171775"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Eglobal, LLC",
      "clearance_type": "Special",
      "date_received": "2017-12-18",
      "decision_code": "SESE",
      "decision_date": "2018-01-26",
      "decision_description": "Substantially Equivalent",
      "device_name": "illumiflow 148 Laser Cap",
      "k_number": "K173843",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K173843"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Chongqing Peninsula Medical Technology Co., Ltd.",
      "clearance_type": "Traditional",
      "date_received": "2017-06-20",
      "decision_code": "SESE",
      "decision_date": "2018-01-30",
      "decision_description": "Substantially Equivalent",
      "device_name": "Irradiation Aesthetic Device",
      "k_number": "K171835",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K171835"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Cosmo Far East Technology Limited",
      "clearance_type": "Traditional",
      "date_received": "2017-11-30",
      "decision_code": "SESE",
      "decision_date": "2018-02-28",
      "decision_description": "Substantially Equivalent",
      "device_name": "Diode Laser Cap",
      "k_number": "K173678",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K173678"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Photonmd, Inc.",
      "clearance_type": "Traditional",
      "date_received": "2017-12-06",
      "decision_code": "SESE",
      "decision_date": "2018-02-28",
      "decision_description": "Substantially Equivalent",
      "device_name": "REVIAN RED",
      "k_number": "K173729",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K173729"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Dermascalp, LLC",
      "clearance_type": "Traditional",
      "date_received": "2017-12-19",
      "decision_code": "SESE",
      "decision_date": "2018-03-21",
      "decision_description": "Substantially Equivalent",
      "device_name": "DermaScalp Laser Cap",
      "k_number": "K173846",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K173846"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Theradome, Inc.",
      "clearance_type": "Traditional",
      "date_received": "2018-02-20",
      "decision_code": "SESE",
      "decision_date": "2018-05-18",
      "decision_description": "Substantially Equivalent",
      "device_name": "Theradome LH40",
      "k_number": "K180460",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K180460"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Y & J Bio Co., Ltd.",
      "clearance_type": "Traditional",
      "date_received": "2018-03-08",
      "decision_code": "SESE",
      "decision_date": "2018-06-01",
      "decision_description": "Substantially Equivalent",
      "device_name": "Hair Up",
      "k_number": "K180617",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K180617"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Lexington International, LLC",
      "clearance_type": "Traditional",
      "date_received": "2018-04-04",
      "decision_code": "SESE",
      "decision_date": "2018-06-20",
      "decision_description": "Substantially Equivalent",
      "device_name": "HairMax Laser",
      "k_number": "K180885",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K180885"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Pjm Worldwide, LLC D/B/A Phoenix Medical Technology, LLC",
      "clearance_type": "Traditional",
      "date_received": "2018-05-11",
      "decision_code": "SESE",
      "decision_date": "2018-08-10",
      "decision_description": "Substantially Equivalent",
      "device_name": "Bosley Revitalizer 272 Laser Cap, Bosley Revitalizer 164 Laser Cup",
      "k_number": "K181253",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K181253"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Super Grow Lasers",
      "clearance_type": "Traditional",
      "date_received": "2018-05-17",
      "decision_code": "SESE",
      "decision_date": "2018-08-15",
      "decision_description": "Substantially Equivalent",
      "device_name": "SuperGrow 272, Ultimate 272",
      "k_number": "K181308",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K181308"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Kiierr International, LLC",
      "clearance_type": "Traditional",
      "date_received": "2018-07-13",
      "decision_code": "SESE",
      "decision_date": "2018-09-05",
      "decision_description": "Substantially Equivalent",
      "device_name": "Kiierr 272 Laser, Kiierr 148 Laser",
      "k_number": "K181878",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K181878"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Pulsaderm, LLC",
      "clearance_type": "Special",
      "date_received": "2018-09-12",
      "decision_code": "SESE",
      "decision_date": "2018-10-26",
      "decision_description": "Substantially Equivalent",
      "device_name": "Hair Laser Headband",
      "k_number": "K182501",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K182501"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Wontech",
      "clearance_type": "Traditional",
      "date_received": "2018-09-18",
      "decision_code": "SESE",
      "decision_date": "2018-11-16",
      "decision_description": "Substantially Equivalent",
      "device_name": "Hair Boom 69",
      "k_number": "K182562",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K182562"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Omm Imports, Inc. D/B/A Zero Gravity",
      "clearance_type": "Traditional",
      "date_received": "2018-11-30",
      "decision_code": "SESE",
      "decision_date": "2019-01-16",
      "decision_description": "Substantially Equivalent",
      "device_name": "Laser Hair Therapy",
      "k_number": "K183329",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K183329"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Freedom Laser Therapy, Inc.",
      "clearance_type": "Traditional",
      "date_received": "2018-12-10",
      "decision_code": "SESE",
      "decision_date": "2019-05-17",
      "decision_description": "Substantially Equivalent",
      "device_name": "iRestore Professional 282",
      "k_number": "K183417",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K183417"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Xuzhou Kernel Medical Equipment Co., Ltd.",
      "clearance_type": "Traditional",
      "date_received": "2019-03-18",
      "decision_code": "SESE",
      "decision_date": "2019-07-26",
      "decision_description": "Substantially Equivalent",
      "device_name": "Hair Growth System",
      "k_number": "K190685",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K190685"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Wontech",
      "clearance_type": "Traditional",
      "date_received": "2019-05-01",
      "decision_code": "SESE",
      "decision_date": "2019-07-29",
      "decision_description": "Substantially Equivalent",
      "device_name": "Hair Boom 69",
      "k_number": "K191154",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K191154"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Capillus",
      "clearance_type": "Special",
      "date_received": "2019-07-29",
      "decision_code": "SESE",
      "decision_date": "2019-09-12",
      "decision_description": "Substantially Equivalent",
      "device_name": "Capillus 112, Capillus 244",
      "k_number": "K192012",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K192012"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Wontech Co., Ltd.",
      "clearance_type": "Special",
      "date_received": "2019-09-05",
      "decision_code": "SESE",
      "decision_date": "2019-09-30",
      "decision_description": "Substantially Equivalent",
      "device_name": "Hair Boom 69, Hair Boom Air, Ulike Hair UpUp",
      "k_number": "K192425",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K192425"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Kunshan Bella Optical Technology Co., Ltd.",
      "clearance_type": "Traditional",
      "date_received": "2019-07-01",
      "decision_code": "SESE",
      "decision_date": "2019-11-22",
      "decision_description": "Substantially Equivalent",
      "device_name": "Hair Growth System",
      "k_number": "K191754",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K191754"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Shang FA Biotechnology Co.",
      "clearance_type": "Traditional",
      "date_received": "2019-09-23",
      "decision_code": "SESE",
      "decision_date": "2019-12-13",
      "decision_description": "Substantially Equivalent",
      "device_name": "Laser Hair Growth Cap",
      "k_number": "K192627",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K192627"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Slinph Technologies Co., Ltd.",
      "clearance_type": "Traditional",
      "date_received": "2019-02-26",
      "decision_code": "SESE",
      "decision_date": "2019-12-26",
      "decision_description": "Substantially Equivalent",
      "device_name": "iHelmet Hair Growth System",
      "k_number": "K190467",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K190467"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Pjm Worldwide, LLC D/B/A Phoenix Medical Technology, LLC",
      "clearance_type": "Special",
      "date_received": "2019-09-19",
      "decision_code": "SESE",
      "decision_date": "2020-01-29",
      "decision_description": "Substantially Equivalent",
      "device_name": "Bosley Revitalizer 96 Laser Cap, Bosley Revitalizer 96 XL Laser Cap",
      "k_number": "K192585",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K192585"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Conversion Labs, Pr, LLC",
      "clearance_type": "Traditional",
      "date_received": "2019-12-31",
      "decision_code": "SESE",
      "decision_date": "2020-03-25",
      "decision_description": "Substantially Equivalent",
      "device_name": "Shapiro MD model laser 272",
      "k_number": "K193667",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K193667"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Chongqing Peninsula Medical Technology Co., Ltd.",
      "clearance_type": "Traditional",
      "date_received": "2019-09-17",
      "decision_code": "SESE",
      "decision_date": "2020-04-17",
      "decision_description": "Substantially Equivalent",
      "device_name": "Irradiation Cosmetic Device",
      "k_number": "K192552",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K192552"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Xuzhou Kernel Medical Equipment Co., Ltd.",
      "clearance_type": "Traditional",
      "date_received": "2020-04-07",
      "decision_code": "SESE",
      "decision_date": "2020-06-03",
      "decision_description": "Substantially Equivalent",
      "device_name": "Hair Growth System",
      "k_number": "K200929",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K200929"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Lg Electronics.Inc",
      "clearance_type": "Traditional",
      "date_received": "2020-02-26",
      "decision_code": "SESE",
      "decision_date": "2020-07-23",
      "decision_description": "Substantially Equivalent",
      "device_name": "LG Pra. L Derma LD Scalp Care",
      "k_number": "K200464",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K200464"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Nature, Inc.redible, Inc.",
      "clearance_type": "Traditional",
      "date_received": "2020-07-06",
      "decision_code": "SESE",
      "decision_date": "2020-09-01",
      "decision_description": "Substantially Equivalent",
      "device_name": "CAPOGEN Laser Cap",
      "k_number": "K201854",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K201854"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Advihair S.R.L.",
      "clearance_type": "Traditional",
      "date_received": "2019-10-28",
      "decision_code": "SESE",
      "decision_date": "2020-12-03",
      "decision_description": "Substantially Equivalent",
      "device_name": "Tricoglam Home Use",
      "k_number": "K193008",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K193008"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Slinph Technologies Co., Ltd.",
      "clearance_type": "Traditional",
      "date_received": "2020-09-11",
      "decision_code": "SESE",
      "decision_date": "2020-12-08",
      "decision_description": "Substantially Equivalent",
      "device_name": "iHelmet Laser Comb",
      "k_number": "K202631",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K202631"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Y & J Bio Co., Ltd.",
      "clearance_type": "Traditional",
      "date_received": "2020-09-30",
      "decision_code": "SESE",
      "decision_date": "2020-12-08",
      "decision_description": "Substantially Equivalent",
      "device_name": "easy Hairfull",
      "k_number": "K202983",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K202983"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Transdermal Cap, Inc.",
      "clearance_type": "Traditional",
      "date_received": "2020-12-29",
      "decision_code": "SESE",
      "decision_date": "2021-03-29",
      "decision_description": "Substantially Equivalent",
      "device_name": "LaserCap Family of Lasers 300, 224, 120 & 80",
      "k_number": "K203826",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K203826"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Dongguan Lescolton Intelligent Electrical Appliance Co., Ltd.",
      "clearance_type": "Traditional",
      "date_received": "2021-01-22",
      "decision_code": "SESE",
      "decision_date": "2021-04-16",
      "decision_description": "Substantially Equivalent",
      "device_name": "Hair Growth Device",
      "k_number": "K210169",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K210169"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Biophotas, Inc.",
      "clearance_type": "Traditional",
      "date_received": "2021-04-07",
      "decision_code": "SESE",
      "decision_date": "2021-06-29",
      "decision_description": "Substantially Equivalent",
      "device_name": "Biophotas Celluma RESTORE",
      "k_number": "K211038",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K211038"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Leana Orders, Inc.",
      "clearance_type": "Traditional",
      "date_received": "2021-04-21",
      "decision_code": "SESE",
      "decision_date": "2021-07-20",
      "decision_description": "Substantially Equivalent",
      "device_name": "Grivamax Family of Lasers, Models 272 and 148",
      "k_number": "K211192",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K211192"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Freedom Laser Therapy, Inc.",
      "clearance_type": "Traditional",
      "date_received": "2021-09-24",
      "decision_code": "SESE",
      "decision_date": "2021-12-22",
      "decision_description": "Substantially Equivalent",
      "device_name": "ID-500 iRestore Hair Growth System",
      "k_number": "K213094",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K213094"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Shenzhen Cosbeauty Technology Co., Ltd.",
      "clearance_type": "Traditional",
      "date_received": "2021-10-25",
      "decision_code": "SESE",
      "decision_date": "2022-01-19",
      "decision_description": "Substantially Equivalent",
      "device_name": "LLLT Laser Hair Growth Cap, Model: Hair Care 88, Hair Care 135, Hair Care 210.",
      "k_number": "K213447",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K213447"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Auxo Hair, LLC",
      "clearance_type": "Traditional",
      "date_received": "2022-02-25",
      "decision_code": "SESE",
      "decision_date": "2022-04-20",
      "decision_description": "Substantially Equivalent",
      "device_name": "Auxo A300, A150 and APod",
      "k_number": "K220543",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K220543"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Kam Yuen Plastic Products , Ltd.",
      "clearance_type": "Traditional",
      "date_received": "2021-09-21",
      "decision_code": "SESE",
      "decision_date": "2022-05-12",
      "decision_description": "Substantially Equivalent",
      "device_name": "Laser hair growth helmet",
      "k_number": "K213025",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K213025"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Kam Yuen Plastic Products , Ltd.",
      "clearance_type": "Traditional",
      "date_received": "2021-09-21",
      "decision_code": "SESE",
      "decision_date": "2022-05-26",
      "decision_description": "Substantially Equivalent",
      "device_name": "Laser Hair Growth Comb",
      "k_number": "K213027",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K213027"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Yibin Yingtong Intelligent Technology Co., Ltd.",
      "clearance_type": "Traditional",
      "date_received": "2021-12-06",
      "decision_code": "SESE",
      "decision_date": "2022-06-24",
      "decision_description": "Substantially Equivalent",
      "device_name": "Intelligence LaserComb",
      "k_number": "K213789",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K213789"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Freedom Laser Therapy, Inc.",
      "clearance_type": "Traditional",
      "date_received": "2022-07-15",
      "decision_code": "SESE",
      "decision_date": "2022-10-13",
      "decision_description": "Substantially Equivalent",
      "device_name": "ID-510 iRestore Elite",
      "k_number": "K222081",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K222081"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Xtrallux, LLC",
      "clearance_type": "Traditional",
      "date_received": "2022-08-04",
      "decision_code": "SESE",
      "decision_date": "2022-11-16",
      "decision_description": "Substantially Equivalent",
      "device_name": "Xtrallux Alpha (XA136R-USA), Xtrallux Super Plus (XS276R-USA/XS276L-USA), Xtrallux Turbo Pro (XP316R-USA), Xtrallux Extreme RX (XR352R-USA)",
      "k_number": "K222364",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K222364"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Dongguan Lescolton Medical Equipment Co., Ltd.",
      "clearance_type": "Traditional",
      "date_received": "2022-08-16",
      "decision_code": "SESE",
      "decision_date": "2022-11-18",
      "decision_description": "Substantially Equivalent",
      "device_name": "Hair Growth Device",
      "k_number": "K222477",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K222477"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Light Tree Ventures Europe B.V.",
      "clearance_type": "Traditional",
      "date_received": "2023-02-07",
      "decision_code": "SESE",
      "decision_date": "2023-04-05",
      "decision_description": "Substantially Equivalent",
      "device_name": "CurrentBody Skin™ Led Hair Regrowth(Model: MZ-07)",
      "k_number": "K230336",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K230336"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Wontech Co., Ltd.",
      "clearance_type": "Special",
      "date_received": "2022-12-23",
      "decision_code": "SESE",
      "decision_date": "2023-04-28",
      "decision_description": "Substantially Equivalent",
      "device_name": "Hair Boom 69, Hair BoomAir, Hair Boom, Ulike Hair UpUp",
      "k_number": "K223862",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K223862"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Light Tree Ventures Europe B.V.",
      "clearance_type": "Traditional",
      "date_received": "2023-03-03",
      "decision_code": "SESE",
      "decision_date": "2023-04-28",
      "decision_description": "Substantially Equivalent",
      "device_name": "Aduro Comb (Model: SZ-22, SZ-22A, SZ-22B)",
      "k_number": "K230597",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K230597"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Hubei Yjt Technology Co.,Ltd",
      "clearance_type": "Traditional",
      "date_received": "2023-01-17",
      "decision_code": "SESE",
      "decision_date": "2023-05-23",
      "decision_description": "Substantially Equivalent",
      "device_name": "Laser Therapy Hair Growth Comb, Model: Lasercomb-001 & Lasercomb-002",
      "k_number": "K230134",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K230134"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Lumenis Be, Ltd.",
      "clearance_type": "Traditional",
      "date_received": "2022-09-15",
      "decision_code": "SESE",
      "decision_date": "2023-06-14",
      "decision_description": "Substantially Equivalent",
      "device_name": "F65 Laser System",
      "k_number": "K222790",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K222790"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Nature, Inc.redible, Inc.",
      "clearance_type": "Traditional",
      "date_received": "2023-04-24",
      "decision_code": "SESE",
      "decision_date": "2023-06-23",
      "decision_description": "Substantially Equivalent",
      "device_name": "Neuhat Hair Growth System; ibeauty.com Laser Cap",
      "k_number": "K231153",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K231153"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Shenzhen Kaiyan Medical Equipment Co., Ltd.",
      "clearance_type": "Traditional",
      "date_received": "2023-05-08",
      "decision_code": "SESE",
      "decision_date": "2023-07-31",
      "decision_description": "Substantially Equivalent",
      "device_name": "Nooance Led And Laser Helmet",
      "k_number": "K231321",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K231321"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Hubei Yjt Technology Co.,Ltd",
      "clearance_type": "Traditional",
      "date_received": "2023-08-07",
      "decision_code": "SESE",
      "decision_date": "2023-10-24",
      "decision_description": "Substantially Equivalent",
      "device_name": "Laser Cap, Model: Hat-01",
      "k_number": "K232356",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K232356"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Wontech Co., Ltd.",
      "clearance_type": "Special",
      "date_received": "2024-01-09",
      "decision_code": "SESE",
      "decision_date": "2024-02-07",
      "decision_description": "Substantially Equivalent",
      "device_name": "Hair Boom Air / Ulike Hair UpUp / Hair Boom 69 / Hair Boom",
      "k_number": "K240064",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K240064"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Plm Worldwide, LLC D/B/A Phoenix Medical Technology, LLC",
      "clearance_type": "Special",
      "date_received": "2024-02-15",
      "decision_code": "SESE",
      "decision_date": "2024-05-22",
      "decision_description": "Substantially Equivalent",
      "device_name": "Bosley Booster 128 Laser Cap; Bosley Booster 162 Laser Cap; Bosley Booster 288 Laser Cap",
      "k_number": "K240456",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K240456"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Revian, Inc.",
      "clearance_type": "Special",
      "date_received": "2024-08-16",
      "decision_code": "SESE",
      "decision_date": "2024-09-13",
      "decision_description": "Substantially Equivalent",
      "device_name": "Revian Lyte (10011)",
      "k_number": "K242441",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K242441"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Telebrands Corporation",
      "clearance_type": "Traditional",
      "date_received": "2024-03-13",
      "decision_code": "SESE",
      "decision_date": "2024-09-17",
      "decision_description": "Substantially Equivalent",
      "device_name": "Robin's Egg",
      "k_number": "K240689",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K240689"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Dongguan Tutamen Metalwork Co., Ltd.",
      "clearance_type": "Traditional",
      "date_received": "2024-02-20",
      "decision_code": "SESE",
      "decision_date": "2024-10-11",
      "decision_description": "Substantially Equivalent",
      "device_name": "PBM Hair Therapy Cap",
      "k_number": "K240472",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K240472"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Shenzhen Breo Technology Co., Ltd.",
      "clearance_type": "Traditional",
      "date_received": "2024-09-03",
      "decision_code": "SESE",
      "decision_date": "2024-11-01",
      "decision_description": "Substantially Equivalent",
      "device_name": "Breo Laser Hair Growth Comb (Scalp 3L)",
      "k_number": "K242620",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K242620"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Shenzhen Nuon Medical Equipment Co., Ltd.",
      "clearance_type": "Traditional",
      "date_received": "2024-05-13",
      "decision_code": "SESE",
      "decision_date": "2024-11-08",
      "decision_description": "Substantially Equivalent",
      "device_name": "Hair Growth Comb (SZ-23,SZ-23A)",
      "k_number": "K241342",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K241342"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Shenzhen Kaiyan Medical Equipment Co., Ltd.",
      "clearance_type": "Traditional",
      "date_received": "2024-08-09",
      "decision_code": "SESE",
      "decision_date": "2024-11-20",
      "decision_description": "Substantially Equivalent",
      "device_name": "HIGHERDOSE Red Light Hat (HG-120K)",
      "k_number": "K242363",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K242363"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Apira Science, Inc.",
      "clearance_type": "Traditional",
      "date_received": "2024-09-03",
      "decision_code": "SESE",
      "decision_date": "2024-12-02",
      "decision_description": "Substantially Equivalent",
      "device_name": "GroWell BT Hair Growth System (GW10042)",
      "k_number": "K242619",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K242619"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Foreo, Inc.",
      "clearance_type": "Traditional",
      "date_received": "2024-09-12",
      "decision_code": "SESE",
      "decision_date": "2024-12-11",
      "decision_description": "Substantially Equivalent",
      "device_name": "FAQ™ (302)",
      "k_number": "K242747",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K242747"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Dongguan Boyuan Intelligent Technology Co.,Ltd",
      "clearance_type": "Traditional",
      "date_received": "2025-02-03",
      "decision_code": "SESE",
      "decision_date": "2025-04-29",
      "decision_description": "Substantially Equivalent",
      "device_name": "Hair Growth Device (KCA441-200, KCA441-120, KCA441-88, KCA441-56, KCA441-200S, KCA441-120S, KCA441-88S, KCA441-56S, KCA451-200, KCA451-120, KCA451-88, KCA451-56, KCA451-200S, KCA451-120S, KCA451-88S, KCA451-56S)",
      "k_number": "K250308",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K250308"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Shenzhen Idea Light Limited",
      "clearance_type": "Traditional",
      "date_received": "2025-02-18",
      "decision_code": "SESE",
      "decision_date": "2025-06-05",
      "decision_description": "Substantially Equivalent",
      "device_name": "Red Light Hair Growth Cap (LP-RJVGRW-BLK)",
      "k_number": "K250467",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K250467"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Shenzhen Kaiyan Medical Equipment Co., Ltd.",
      "clearance_type": "Traditional",
      "date_received": "2025-04-02",
      "decision_code": "SESE",
      "decision_date": "2025-06-17",
      "decision_description": "Substantially Equivalent",
      "device_name": "CurrentBody Skin Dual Light Hair Growth Helmet (model: MZ-07A)",
      "k_number": "K251017",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K251017"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Cosmo Far East Technology Limited",
      "clearance_type": "Traditional",
      "date_received": "2025-07-25",
      "decision_code": "SESE",
      "decision_date": "2025-10-22",
      "decision_description": "Substantially Equivalent",
      "device_name": "Hair Growth Laser Cap",
      "k_number": "K252325",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K252325"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Shenzhen Kaiyan Medical Equipment Co., Ltd.",
      "clearance_type": "Traditional",
      "date_received": "2025-08-01",
      "decision_code": "SESE",
      "decision_date": "2025-10-30",
      "decision_description": "Substantially Equivalent",
      "device_name": "Q-Renew LLLT Hair Growth Helmet (Q-HLMT-V1)",
      "k_number": "K252414",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K252414"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Light Tree Ventures Europe B.V.",
      "clearance_type": "Traditional",
      "date_received": "2025-09-30",
      "decision_code": "SESE",
      "decision_date": "2025-12-24",
      "decision_description": "Substantially Equivalent",
      "device_name": "Hair Regrowth Cap (Model: T-119-HRC)",
      "k_number": "K253349",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K253349"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Shenzhen Kaiyan Medical Equipment Co., Ltd.",
      "clearance_type": "Traditional",
      "date_received": "2025-11-21",
      "decision_code": "SESE",
      "decision_date": "2026-01-23",
      "decision_description": "Substantially Equivalent",
      "device_name": "TRUDERMAL HALO HAIR GROWTH SYSTEM (M-180A); ADURO HAIR GROWTH (M-130,M-300)",
      "k_number": "K253669",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K253669"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Alma Lasers, Inc.",
      "clearance_type": "Traditional",
      "date_received": "2025-06-02",
      "decision_code": "SESE",
      "decision_date": "2026-06-05",
      "decision_description": "Substantially Equivalent",
      "device_name": "Alma TED+ System",
      "k_number": "K251684",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K251684"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Hubei Yjt Technology Co.,Ltd",
      "clearance_type": "Traditional",
      "date_received": "2025-09-29",
      "decision_code": "SESE",
      "decision_date": "2026-06-16",
      "decision_description": "Substantially Equivalent",
      "device_name": "Laser Hair Growth System (Laser Cap 128, Laser Helmet 272, Laser Helmet 352, Laser Helmet 552, Laser Helmet 500)",
      "k_number": "K253231",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K253231"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Zdeer Technology (Henan) Co., Ltd.",
      "clearance_type": "Traditional",
      "date_received": "2026-03-18",
      "decision_code": "SESE",
      "decision_date": "2026-06-16",
      "decision_description": "Substantially Equivalent",
      "device_name": "Laser Hair Growth Device (F21151, F21152, F21153, F21154, F21155, F21156, F21157, F21158, F21159)",
      "k_number": "K260899",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K260899"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Ziree Co., Ltd.",
      "clearance_type": "Traditional",
      "date_received": "2026-04-16",
      "decision_code": "SESE",
      "decision_date": "2026-06-26",
      "decision_description": "Substantially Equivalent",
      "device_name": "Laser Hair Growth Devices (HR-H1, HR-H2, HR-H3, HR-H4, HR-H5, HR-H6, HR-H7, HR-H8, HR-H9, HR-H10, HR-I1, HR-I2, HR-I3, HR-I4, HR-I5)",
      "k_number": "K261253",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K261253"
    },
    {
      "advisory_committee_description": "Physical Medicine",
      "applicant": "Shenzhen Chuanghong Zhilian Technology Co., Ltd.",
      "clearance_type": "Traditional",
      "date_received": "2026-05-21",
      "decision_code": "SESE",
      "decision_date": "2026-07-17",
      "decision_description": "Substantially Equivalent",
      "device_name": "CHZL Red Light Therapy Hair Growth Cap (Model(s):CHZL-120BK-L52D,CHZL-120BK-L53D,CHZL-120BK-L54D)",
      "k_number": "K261675",
      "product_code": "OAP",
      "fda_record_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K261675"
    }
  ]
}