{
  "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": 1
    }
  },
  "results": [
    {
      "proprietary_name": [],
      "establishment_type": [
        "Repack or Relabel Medical Device"
      ],
      "registration": {
        "registration_number": "3038776570",
        "fei_number": "3038776570",
        "status_code": "1",
        "initial_importer_flag": "Y",
        "reg_expiry_date_year": "2026",
        "name": "INVOSURG INC",
        "address_line_1": "480 Neponset St Ste 11b",
        "address_line_2": "",
        "city": "Canton",
        "state_code": "MA",
        "iso_country_code": "US",
        "zip_code": "02021",
        "postal_code": "",
        "us_agent": {},
        "owner_operator": {
          "firm_name": "Invosurg Inc",
          "owner_operator_number": "10093658",
          "official_correspondent": {
            "first_name": "RICHARD",
            "middle_initial": "",
            "last_name": "WALCZAK",
            "subaccount_company_name": "",
            "phone_number": "001-919-4513007-x"
          },
          "contact_address": {
            "address_1": "480 neponset street",
            "address_2": "Building 11B",
            "city": "Canton",
            "state_code": "MA",
            "state_province": "",
            "iso_country_code": "US",
            "postal_code": "02021"
          }
        }
      },
      "pma_number": "",
      "k_number": "K180453",
      "products": [
        {
          "product_code": "DWF",
          "created_date": "2025-06-17",
          "owner_operator_number": "10093658",
          "exempt": "",
          "openfda": {
            "device_name": "Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass",
            "medical_specialty_description": "Cardiovascular",
            "regulation_number": "870.4210",
            "device_class": "2"
          }
        }
      ]
    }
  ]
}