{
  "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": [
        "MED TECH EXTREMITY SPLINT"
      ],
      "establishment_type": [
        "Manufacture Medical Device"
      ],
      "registration": {
        "registration_number": "3007407648",
        "fei_number": "3007407648",
        "status_code": "1",
        "initial_importer_flag": "N",
        "reg_expiry_date_year": "2026",
        "name": "RED MEDICAL CORPORATION dba Med Tech Sweden Inc (Unit # 4, 3 and Office)",
        "address_line_1": "320 Weber Dr Ste 4",
        "address_line_2": "",
        "city": "Geneseo",
        "state_code": "IL",
        "iso_country_code": "US",
        "zip_code": "61254",
        "postal_code": "",
        "us_agent": {},
        "owner_operator": {
          "firm_name": "Red Medical Corp. dba Med Tech Sweden",
          "owner_operator_number": "10028340",
          "official_correspondent": {
            "first_name": "Tracy",
            "middle_initial": "M",
            "last_name": "Renberg",
            "subaccount_company_name": "",
            "phone_number": "x-309-8537724-x"
          },
          "contact_address": {
            "address_1": "320 Weber Drive Unit 4",
            "address_2": "",
            "city": "Geneseo",
            "state_code": "IL",
            "state_province": "",
            "iso_country_code": "US",
            "postal_code": "61254"
          }
        }
      },
      "pma_number": "",
      "k_number": "",
      "products": [
        {
          "product_code": "NOC",
          "created_date": "2009-01-21",
          "owner_operator_number": "10028340",
          "exempt": "",
          "openfda": {
            "device_name": "Splint, Extremity, Non-Inflatable, External, Non-Sterile",
            "medical_specialty_description": "General, Plastic Surgery",
            "regulation_number": "878.3910",
            "device_class": "1"
          }
        }
      ]
    }
  ]
}