{
  "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": "2026-07-20",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "third_party_flag": "N",
      "life_sustain_support_flag": "N",
      "gmp_exempt_flag": "N",
      "summary_malfunction_reporting": "Ineligible",
      "product_code": "QIU",
      "openfda": {
        "k_number": [
          "DEN200028"
        ],
        "registration_number": [
          "2953684",
          "3009040934",
          "3021349626"
        ],
        "fei_number": [
          "3009040934",
          "3001611958",
          "3021349626"
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      },
      "review_panel": "OP",
      "medical_specialty": "OP",
      "device_name": "Intense Pulsed Light Device For Managing Dry Eye",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "Ophthalmic",
      "device_class": "2",
      "definition": "An intense pulsed light device for managing dry eye is a prescription device intended for use in the application of intense pulsed light therapy to the skin. The device is used in patients with dry eye disease due to meibomian gland dysfunction, also known as evaporative dry eye or lipid deficiency dry eye.",
      "regulation_number": "886.5201",
      "implant_flag": "N",
      "submission_type_id": "1"
    }
  ]
}