{
  "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": 4
    }
  },
  "results": [
    {
      "proprietary_name": [],
      "establishment_type": [
        "Reprocess Single-Use Device"
      ],
      "registration": {
        "registration_number": "3015988948",
        "fei_number": "3015988948",
        "status_code": "1",
        "initial_importer_flag": "N",
        "reg_expiry_date_year": "2027",
        "name": "VEIN360",
        "address_line_1": "4460 Lake Forest Dr",
        "address_line_2": "STE 218",
        "city": "Blue Ash",
        "state_code": "OH",
        "iso_country_code": "US",
        "zip_code": "45242",
        "postal_code": "",
        "us_agent": {},
        "owner_operator": {
          "firm_name": "Vein360",
          "owner_operator_number": "10061626",
          "official_correspondent": {
            "first_name": "Suzanne",
            "middle_initial": "",
            "last_name": "Meyer",
            "subaccount_company_name": "",
            "phone_number": "1-513-5541300-x"
          },
          "contact_address": {
            "address_1": "4460 LAKE FOREST DR",
            "address_2": "STE 218",
            "city": "Cincinnati",
            "state_code": "OH",
            "state_province": "",
            "iso_country_code": "US",
            "postal_code": "45242"
          }
        }
      },
      "pma_number": "",
      "k_number": "K191073",
      "products": [
        {
          "product_code": "NUJ",
          "created_date": "2019-11-04",
          "owner_operator_number": "10061626",
          "exempt": "",
          "openfda": {
            "device_name": "Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed",
            "medical_specialty_description": "General, Plastic Surgery",
            "regulation_number": "878.4400",
            "device_class": "2"
          }
        },
        {
          "product_code": "GEI",
          "created_date": "2019-11-04",
          "owner_operator_number": "10061626",
          "exempt": "",
          "openfda": {
            "device_name": "Electrosurgical, Cutting & Coagulation & Accessories",
            "medical_specialty_description": "General, Plastic Surgery",
            "regulation_number": "878.4400",
            "device_class": "2"
          }
        }
      ]
    }
  ]
}