{
  "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": 136
    }
  },
  "results": [
    {
      "proprietary_name": [
        "Consulta CRT-P",
        "Attain Bipolar OTW Lead",
        "Serena Quad CRT-P MRI SureScan",
        "Percepta Quad CRT-P MRI SureScan",
        "Percepta CRT-P MRI SureScan",
        "Syncra CRT-P",
        "Viva CRT-P",
        "Attain OTW",
        "Insync",
        "Attain",
        "Solara CRT-P MRI SureScan",
        "Serena CRT-P MRI SureScan",
        "Solara Quad CRT-P MRI SureScan",
        "CareLink SmartSync Percepta, Solera, Serena Application"
      ],
      "establishment_type": [
        "Develop Specifications But Do Not Manufacture At This Facility",
        "Manufacture Medical Device"
      ],
      "registration": {
        "registration_number": "2182208",
        "fei_number": "2182208",
        "status_code": "1",
        "initial_importer_flag": "N",
        "reg_expiry_date_year": "2027",
        "name": "MEDTRONIC, INC.",
        "address_line_1": "8200 Coral Sea Street NE",
        "address_line_2": "",
        "city": "Mounds View",
        "state_code": "MN",
        "iso_country_code": "US",
        "zip_code": "55112",
        "postal_code": "",
        "us_agent": {},
        "owner_operator": {
          "firm_name": "Medtronic, Inc.",
          "owner_operator_number": "2112641",
          "official_correspondent": {},
          "contact_address": {
            "address_1": "710 Medtronic Parkway",
            "address_2": "",
            "city": "Minneapolis",
            "state_code": "MN",
            "state_province": "",
            "iso_country_code": "US",
            "postal_code": "55432"
          }
        }
      },
      "pma_number": "P010015",
      "k_number": "",
      "products": [
        {
          "product_code": "LWP",
          "created_date": "2007-01-23",
          "owner_operator_number": "2112641",
          "exempt": "",
          "openfda": {
            "device_name": "Implantable Pulse Generator, Pacemaker (Non-Crt)",
            "medical_specialty_description": "Unknown",
            "regulation_number": "",
            "device_class": "3"
          }
        },
        {
          "product_code": "OJX",
          "created_date": "2007-01-23",
          "owner_operator_number": "2112641",
          "exempt": "",
          "openfda": {
            "pma_number": [
              "P010015"
            ],
            "device_name": "Drug Eluting Permanent Left Ventricular (Lv) Pacemaker Electrode",
            "medical_specialty_description": "Unknown",
            "regulation_number": "",
            "device_class": "3"
          }
        },
        {
          "product_code": "NVZ",
          "created_date": "2007-01-23",
          "owner_operator_number": "2112641",
          "exempt": "",
          "openfda": {
            "device_name": "Pulse Generator, Permanent, Implantable",
            "medical_specialty_description": "Unknown",
            "regulation_number": "",
            "device_class": "3"
          }
        },
        {
          "product_code": "NKE",
          "created_date": "2007-01-23",
          "owner_operator_number": "2112641",
          "exempt": "",
          "openfda": {
            "device_name": "Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)",
            "medical_specialty_description": "Unknown",
            "regulation_number": "",
            "device_class": "3"
          }
        }
      ]
    }
  ]
}