{
  "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": 6
    }
  },
  "results": [
    {
      "proprietary_name": [
        "Epiphany PSL Cage",
        "Epiphany PSE Cage"
      ],
      "establishment_type": [
        "Manufacture Medical Device for Another Party (Contract Manufacturer)"
      ],
      "registration": {
        "registration_number": "3010143171",
        "fei_number": "3010143171",
        "status_code": "1",
        "initial_importer_flag": "N",
        "reg_expiry_date_year": "2026",
        "name": "AR FABRICATING",
        "address_line_1": "40132 Industrial Park Cir Ste 102",
        "address_line_2": "",
        "city": "Georgetown",
        "state_code": "TX",
        "iso_country_code": "US",
        "zip_code": "78626",
        "postal_code": "",
        "us_agent": {},
        "owner_operator": {
          "firm_name": "AR Fabricating",
          "owner_operator_number": "10043437",
          "official_correspondent": {
            "first_name": "Thomas",
            "middle_initial": "",
            "last_name": "Siemer",
            "subaccount_company_name": "",
            "phone_number": "01-512-2404246-x"
          },
          "contact_address": {
            "address_1": "40132 Industrial park Cir.",
            "address_2": "suite 102",
            "city": "Georgetown",
            "state_code": "TX",
            "state_province": "",
            "iso_country_code": "US",
            "postal_code": "78626"
          }
        }
      },
      "pma_number": "",
      "k_number": "",
      "products": [
        {
          "product_code": "MAX",
          "created_date": "2019-01-24",
          "owner_operator_number": "10043437",
          "exempt": "",
          "openfda": {
            "device_name": "Intervertebral Fusion Device With Bone Graft, Lumbar",
            "medical_specialty_description": "Orthopedic",
            "regulation_number": "888.3080",
            "device_class": "2"
          }
        }
      ]
    }
  ]
}