{
  "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": "2026-10-12",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 5
    }
  },
  "results": [
    {
      "proprietary_name": [
        "Scatterguard"
      ],
      "establishment_type": [
        "Develop Specifications But Do Not Manufacture At This Facility"
      ],
      "registration": {
        "registration_number": "1063300",
        "fei_number": "1000488948",
        "status_code": "1",
        "initial_importer_flag": "N",
        "reg_expiry_date_year": "2027",
        "name": "PROTECH LEADED EYEWEAR, INC.",
        "address_line_1": "7960 Central Industrial Drive",
        "address_line_2": "Ste 125",
        "city": "West Palm Beach",
        "state_code": "FL",
        "iso_country_code": "US",
        "zip_code": "33404",
        "postal_code": "",
        "us_agent": {},
        "owner_operator": {
          "firm_name": "Protech Leaded Eyewear, Inc.",
          "owner_operator_number": "10025412",
          "official_correspondent": {
            "first_name": "Evin",
            "middle_initial": "",
            "last_name": "Lalan",
            "subaccount_company_name": "",
            "phone_number": "1-561-6279769-x"
          },
          "contact_address": {
            "address_1": "7960 Central Industrial Drive",
            "address_2": "Ste 125",
            "city": "West Palm Beach",
            "state_code": "FL",
            "state_province": "",
            "iso_country_code": "US",
            "postal_code": "33404"
          }
        }
      },
      "pma_number": "",
      "k_number": "",
      "products": [
        {
          "product_code": "PUI",
          "created_date": "2023-10-09",
          "owner_operator_number": "10025412",
          "exempt": "",
          "openfda": {
            "device_name": "Drape, Surgical, Exempt",
            "medical_specialty_description": "General, Plastic Surgery",
            "regulation_number": "878.4370",
            "device_class": "2"
          }
        }
      ]
    }
  ]
}