{
  "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": "2026-10-19",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 2
    }
  },
  "results": [
    {
      "proprietary_name": [],
      "establishment_type": [
        "Develop Specifications But Do Not Manufacture At This Facility"
      ],
      "registration": {
        "registration_number": "3013613028",
        "fei_number": "3013613028",
        "status_code": "1",
        "initial_importer_flag": "Y",
        "reg_expiry_date_year": "2026",
        "name": "CATH DRY GLOBAL, INC",
        "address_line_1": "1243 North Hoover Street",
        "address_line_2": "",
        "city": "Los Angeles",
        "state_code": "CA",
        "iso_country_code": "US",
        "zip_code": "90029",
        "postal_code": "",
        "us_agent": {},
        "owner_operator": {
          "firm_name": "Cath Dry, Inc",
          "owner_operator_number": "10085908",
          "official_correspondent": {
            "first_name": "Pascal",
            "middle_initial": "",
            "last_name": "Dabel",
            "subaccount_company_name": "",
            "phone_number": "x-781-8669875-x"
          },
          "contact_address": {
            "address_1": "1243 North Hoover Street",
            "address_2": "",
            "city": "Los Angeles",
            "state_code": "CA",
            "state_province": "",
            "iso_country_code": "US",
            "postal_code": "90029"
          }
        }
      },
      "pma_number": "",
      "k_number": "",
      "products": [
        {
          "product_code": "KMK",
          "created_date": "2022-09-04",
          "owner_operator_number": "10085908",
          "exempt": "",
          "openfda": {
            "device_name": "Device, Intravascular Catheter Securement",
            "medical_specialty_description": "General Hospital",
            "regulation_number": "880.5210",
            "device_class": "1"
          }
        }
      ]
    }
  ]
}