{
  "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": "2026-09-07",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 2
    }
  },
  "results": [
    {
      "proprietary_name": [
        "DOLFINO GOGGLE"
      ],
      "establishment_type": [
        "Manufacture Medical Device for Another Party (Contract Manufacturer)"
      ],
      "registration": {
        "registration_number": "3000159466",
        "fei_number": "3000159466",
        "status_code": "1",
        "initial_importer_flag": "Y",
        "reg_expiry_date_year": "2026",
        "name": "KWIK TEK, INC.",
        "address_line_1": "12000 E 45th Ave",
        "address_line_2": "",
        "city": "Denver",
        "state_code": "CO",
        "iso_country_code": "US",
        "zip_code": "80239",
        "postal_code": "",
        "us_agent": {},
        "owner_operator": {
          "firm_name": "AQUA LEISURE RECREATION LLC",
          "owner_operator_number": "1221480",
          "official_correspondent": {
            "first_name": "BONNIE",
            "middle_initial": "-",
            "last_name": "FEIGHT",
            "subaccount_company_name": "",
            "phone_number": "x-303-7333722-x"
          },
          "contact_address": {
            "address_1": "100 TECHNOLOGY CENTER DRIVE",
            "address_2": "SUITE 500",
            "city": "Stoughton",
            "state_code": "MA",
            "state_province": "",
            "iso_country_code": "US",
            "postal_code": "02072"
          }
        }
      },
      "pma_number": "",
      "k_number": "",
      "products": [
        {
          "product_code": "HOY",
          "created_date": "2005-10-20",
          "owner_operator_number": "1221480",
          "exempt": "",
          "openfda": {
            "device_name": "Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)",
            "medical_specialty_description": "Ophthalmic",
            "regulation_number": "886.4750",
            "device_class": "1"
          }
        }
      ]
    }
  ]
}