{
  "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": "2026-08-03",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 20
    }
  },
  "results": [
    {
      "proprietary_name": [],
      "establishment_type": [
        "Manufacture Medical Device for Another Party (Contract Manufacturer)"
      ],
      "registration": {
        "registration_number": "3006990600",
        "fei_number": "3006990600",
        "status_code": "1",
        "initial_importer_flag": "N",
        "reg_expiry_date_year": "2026",
        "name": "Arthrex California Technology, Incorporated",
        "address_line_1": "460 Ward Dr",
        "address_line_2": "",
        "city": "Santa Barbara",
        "state_code": "CA",
        "iso_country_code": "US",
        "zip_code": "93111",
        "postal_code": "",
        "us_agent": {},
        "owner_operator": {
          "firm_name": "ARTHREX, INC.",
          "owner_operator_number": "1220287",
          "official_correspondent": {
            "first_name": "Barry",
            "middle_initial": "",
            "last_name": "Dietz",
            "subaccount_company_name": "",
            "phone_number": "1-800-9337001-76939"
          },
          "contact_address": {
            "address_1": "1370 CREEKSIDE BLVD.",
            "address_2": "--",
            "city": "Naples",
            "state_code": "FL",
            "state_province": "",
            "iso_country_code": "US",
            "postal_code": "34108"
          }
        }
      },
      "pma_number": "",
      "k_number": "",
      "products": [
        {
          "product_code": "QHE",
          "created_date": "2024-05-23",
          "owner_operator_number": "1220287",
          "exempt": "",
          "openfda": {
            "device_name": "Shoulder Arthroplasty Implantation System",
            "medical_specialty_description": "Orthopedic",
            "regulation_number": "888.3660",
            "device_class": "2"
          }
        }
      ]
    }
  ]
}