{
  "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": "Ineligible",
      "product_code": "PZK",
      "openfda": {
        "pma_number": [
          "P160055"
        ],
        "registration_number": [
          "2030624",
          "3012712027"
        ],
        "fei_number": [
          "3000206435",
          "3012712027"
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      },
      "review_panel": "OP",
      "medical_specialty": "OP",
      "device_name": "Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "Ophthalmic",
      "device_class": "3",
      "definition": "The system consists of an intraocular lens and an external energy source. The lens is intended to be implanted to replace the natural lens of an eye. The external energy source is used to postoperatively alter the properties of the lens material to reduce the likelihood of clinically significant postoperative refractive error.",
      "regulation_number": "886.3600",
      "implant_flag": "Y",
      "submission_type_id": "2"
    }
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}