{
  "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": 4
    }
  },
  "results": [
    {
      "proprietary_name": [],
      "establishment_type": [
        "Manufacture Medical Device for Another Party (Contract Manufacturer)"
      ],
      "registration": {
        "registration_number": "3016020790",
        "fei_number": "3016020790",
        "status_code": "1",
        "initial_importer_flag": "N",
        "reg_expiry_date_year": "2026",
        "name": "MEDDUX DEVELOPMENT CORPORATION LLC",
        "address_line_1": "6165 Lookout Rd",
        "address_line_2": "",
        "city": "Boulder",
        "state_code": "CO",
        "iso_country_code": "US",
        "zip_code": "80301",
        "postal_code": "",
        "us_agent": {},
        "owner_operator": {
          "firm_name": "Meddux Development Corporation LLC",
          "owner_operator_number": "10083304",
          "official_correspondent": {
            "first_name": "Chad",
            "middle_initial": "",
            "last_name": "Herremans",
            "subaccount_company_name": "",
            "phone_number": "1-720-6757154-x"
          },
          "contact_address": {
            "address_1": "6165 Lookout Rd",
            "address_2": "",
            "city": "Boulder",
            "state_code": "CO",
            "state_province": "",
            "iso_country_code": "US",
            "postal_code": "80301"
          }
        }
      },
      "pma_number": "",
      "k_number": "",
      "products": [
        {
          "product_code": "GEI",
          "created_date": "2024-05-31",
          "owner_operator_number": "10083304",
          "exempt": "",
          "openfda": {
            "device_name": "Electrosurgical, Cutting & Coagulation & Accessories",
            "medical_specialty_description": "General, Plastic Surgery",
            "regulation_number": "878.4400",
            "device_class": "2"
          }
        },
        {
          "product_code": "OAB",
          "created_date": "2024-05-31",
          "owner_operator_number": "10083304",
          "exempt": "",
          "openfda": {
            "device_name": "Low Energy Direct Current Thermal Ablation System",
            "medical_specialty_description": "General, Plastic Surgery",
            "regulation_number": "878.4400",
            "device_class": "2"
          }
        }
      ]
    }
  ]
}