{
  "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": 2
    }
  },
  "results": [
    {
      "proprietary_name": [
        "DA-2006-VL"
      ],
      "establishment_type": [
        "Manufacture Medical Device"
      ],
      "registration": {
        "registration_number": "2939012",
        "fei_number": "2939012",
        "status_code": "1",
        "initial_importer_flag": "N",
        "reg_expiry_date_year": "2026",
        "name": "BC GROUP INTERNATIONAL, INC.",
        "address_line_1": "3081 Elm Point Industrial Dr",
        "address_line_2": "",
        "city": "Saint Charles",
        "state_code": "MO",
        "iso_country_code": "US",
        "zip_code": "63301",
        "postal_code": "",
        "us_agent": {},
        "owner_operator": {
          "firm_name": "BC Group International, Inc.",
          "owner_operator_number": "10037117",
          "official_correspondent": {
            "first_name": "Mel",
            "middle_initial": "",
            "last_name": "Roche",
            "subaccount_company_name": "",
            "phone_number": "x-314-6383800-x"
          },
          "contact_address": {
            "address_1": "3081 Elm Point Industrial Drive",
            "address_2": "",
            "city": "Saint Charles",
            "state_code": "MO",
            "state_province": "",
            "iso_country_code": "US",
            "postal_code": "63301"
          }
        }
      },
      "pma_number": "",
      "k_number": "K153210",
      "products": [
        {
          "product_code": "DRL",
          "created_date": "2016-09-19",
          "owner_operator_number": "10037117",
          "exempt": "",
          "openfda": {
            "k_number": [
              "K153210"
            ],
            "device_name": "Tester, Defibrillator",
            "medical_specialty_description": "Cardiovascular",
            "regulation_number": "870.5325",
            "device_class": "2"
          }
        }
      ]
    }
  ]
}