{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-07-27",
    "results": {
      "skip": 0,
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  "results": [
    {
      "third_party_flag": "N",
      "city": "Laval",
      "advisory_committee_description": "General, Plastic Surgery",
      "address_1": "275, Boul. Armand Frappier",
      "address_2": "",
      "statement_or_summary": "",
      "product_code": "QPE",
      "openfda": {
        "device_name": "Phototherapy Device For Reducing The Appearance Of Acute Post-Surgical Incisions",
        "medical_specialty_description": "General, Plastic Surgery",
        "regulation_number": "878.4880",
        "device_class": "2"
      },
      "zip_code": "H7V 4A7",
      "applicant": "Klox Technlogies, Inc.",
      "decision_date": "2021-12-03",
      "decision_code": "DENG",
      "country_code": "CA",
      "device_name": "Klox Biophotonic LumiHeal System",
      "advisory_committee": "SU",
      "contact": "Daniela  Jukic",
      "expedited_review_flag": "",
      "k_number": "DEN200005",
      "state": "",
      "date_received": "2020-02-04",
      "review_advisory_committee": "SU",
      "postal_code": "H7V 4A7",
      "decision_description": "Unknown",
      "clearance_type": "Direct"
    }
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}