{
  "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": "2026-11-02",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "third_party_flag": "N",
      "life_sustain_support_flag": "N",
      "gmp_exempt_flag": "N",
      "summary_malfunction_reporting": "Eligible",
      "product_code": "NIZ",
      "openfda": {},
      "review_panel": "OP",
      "medical_specialty": "OP",
      "device_name": "Lens, Iris Reconstruction",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "Ophthalmic",
      "device_class": "3",
      "definition": "An iris reconstruction lens is an intraocular lens (IOL) which is used in patients with partial  or complete loss of the iris induced by trauma or congenital defect. The IOL serves as an artificial iris and lens,  reducing light sensitivity and/or glare disability. The device is implanted in the capsular bag or sulcus for the correction  of aphakia and aniridia.",
      "regulation_number": "886.3600",
      "implant_flag": "Y",
      "submission_type_id": "2"
    }
  ]
}