{
  "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": "2026-08-03",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 6
    }
  },
  "results": [
    {
      "proprietary_name": [
        "Mark 5 Nuvo Lite STD (520, 920)",
        "Mark 5 Nuvo Lite OCSI (525, 925)",
        "Mark 5 Nuvo Lite 3 (935)",
        "GCE Mediline Nuvo Lite (925GC)"
      ],
      "establishment_type": [
        "Manufacture Medical Device"
      ],
      "registration": {
        "registration_number": "1039215",
        "fei_number": "1039215",
        "status_code": "1",
        "initial_importer_flag": "N",
        "reg_expiry_date_year": "2026",
        "name": "NIDEK MEDICAL PRODUCTS, INC.",
        "address_line_1": "3949 VALLEY EAST INDUSTRIAL DR",
        "address_line_2": "",
        "city": "Birmingham",
        "state_code": "AL",
        "iso_country_code": "US",
        "zip_code": "35217",
        "postal_code": "",
        "us_agent": {},
        "owner_operator": {
          "firm_name": "NIDEK MEDICAL PRODUCTS, INC.",
          "owner_operator_number": "1039215",
          "official_correspondent": {
            "first_name": "Olivia",
            "middle_initial": "H",
            "last_name": "Mullen",
            "subaccount_company_name": "",
            "phone_number": "x-205-8567200-220"
          },
          "contact_address": {
            "address_1": "3949 VALLEY EAST INDUSTRIAL DR",
            "address_2": "--",
            "city": "Birmingham",
            "state_code": "AL",
            "state_province": "",
            "iso_country_code": "US",
            "postal_code": "35217"
          }
        }
      },
      "pma_number": "",
      "k_number": "K123738",
      "products": [
        {
          "product_code": "CAW",
          "created_date": "2015-10-27",
          "owner_operator_number": "1039215",
          "exempt": "",
          "openfda": {
            "device_name": "Generator, Oxygen, Portable",
            "medical_specialty_description": "Anesthesiology",
            "regulation_number": "868.5440",
            "device_class": "2"
          }
        }
      ]
    }
  ]
}