{
  "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": 3
    }
  },
  "results": [
    {
      "proprietary_name": [
        "Impression Material"
      ],
      "establishment_type": [
        "Repack or Relabel Medical Device"
      ],
      "registration": {
        "registration_number": "2094377",
        "fei_number": "2094377",
        "status_code": "1",
        "initial_importer_flag": "N",
        "reg_expiry_date_year": "2026",
        "name": "WESTONE LABORATORIES, INC.",
        "address_line_1": "2260 Executive Cirle",
        "address_line_2": "",
        "city": "Colorado Springs",
        "state_code": "CO",
        "iso_country_code": "US",
        "zip_code": "80906",
        "postal_code": "",
        "us_agent": {},
        "owner_operator": {
          "firm_name": "WESTONE LABORATORIES, INC.",
          "owner_operator_number": "9027818",
          "official_correspondent": {
            "first_name": "Vanessa",
            "middle_initial": "",
            "last_name": "Webster",
            "subaccount_company_name": "",
            "phone_number": "1-719-4345324-x"
          },
          "contact_address": {
            "address_1": "2260 EXECUTIVE CIRCLE",
            "address_2": "",
            "city": "Colorado Springs",
            "state_code": "CO",
            "state_province": "",
            "iso_country_code": "US",
            "postal_code": "80906"
          }
        }
      },
      "pma_number": "",
      "k_number": "",
      "products": [
        {
          "product_code": "LDG",
          "created_date": "2017-11-27",
          "owner_operator_number": "9027818",
          "exempt": "",
          "openfda": {
            "device_name": "Kit, Earmold, Impression",
            "medical_specialty_description": "Ear, Nose, Throat",
            "regulation_number": "874.3300",
            "device_class": "1"
          }
        }
      ]
    }
  ]
}