{
  "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,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "third_party_flag": "N",
      "life_sustain_support_flag": "N",
      "gmp_exempt_flag": "N",
      "summary_malfunction_reporting": "Ineligible",
      "product_code": "QMM",
      "openfda": {
        "k_number": [
          "DEN200002"
        ],
        "registration_number": [
          "3012862899"
        ],
        "fei_number": [
          "3012862899"
        ]
      },
      "review_panel": "OP",
      "medical_specialty": "OP",
      "device_name": "Hydrophilic Re-Coating Solution",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "Ophthalmic",
      "device_class": "2",
      "definition": "A hydrophilic re-coating solution is a home use device intended to restore the hydrophilic coating of rigid gas permeable (RGP) contact lenses using reactive coating components. For prescription use only.",
      "regulation_number": "886.5919",
      "implant_flag": "N",
      "submission_type_id": "1"
    }
  ]
}