{
  "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": "2026-10-26",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 3
    }
  },
  "results": [
    {
      "proprietary_name": [
        "Neulight®"
      ],
      "establishment_type": [
        "Manufacture Medical Device"
      ],
      "registration": {
        "registration_number": "3007336385",
        "fei_number": "3007336385",
        "status_code": "1",
        "initial_importer_flag": "N",
        "reg_expiry_date_year": "2026",
        "name": "WEINERT Fiber Optics Inc.",
        "address_line_1": "209 Bulifants Blvd",
        "address_line_2": "",
        "city": "Williamsburg",
        "state_code": "VA",
        "iso_country_code": "US",
        "zip_code": "23188",
        "postal_code": "",
        "us_agent": {},
        "owner_operator": {
          "firm_name": "WEINERT Fiber Optics, Inc.",
          "owner_operator_number": "10085607",
          "official_correspondent": {
            "first_name": "Phillip",
            "middle_initial": "",
            "last_name": "LaCroix",
            "subaccount_company_name": "",
            "phone_number": "x-757-2584805-510"
          },
          "contact_address": {
            "address_1": "209 Bulifants Blvd.",
            "address_2": "",
            "city": "Williamsburg",
            "state_code": "VA",
            "state_province": "",
            "iso_country_code": "US",
            "postal_code": "23188"
          }
        }
      },
      "pma_number": "",
      "k_number": "K201171",
      "products": [
        {
          "product_code": "GEX",
          "created_date": "2022-07-08",
          "owner_operator_number": "10085607",
          "exempt": "",
          "openfda": {
            "device_name": "Powered Laser Surgical Instrument",
            "medical_specialty_description": "General, Plastic Surgery",
            "regulation_number": "878.4810",
            "device_class": "2"
          }
        }
      ]
    }
  ]
}