{
  "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": 55
    }
  },
  "results": [
    {
      "proprietary_name": [
        "Modification of RD Single"
      ],
      "establishment_type": [
        "Manufacture Medical Device"
      ],
      "registration": {
        "registration_number": "3011936113",
        "fei_number": "3011936113",
        "status_code": "1",
        "initial_importer_flag": "Y",
        "reg_expiry_date_year": "2026",
        "name": "Keystone Dental Inc.",
        "address_line_1": "13645 Alton Pkwy Ste A",
        "address_line_2": "",
        "city": "Irvine",
        "state_code": "CA",
        "iso_country_code": "US",
        "zip_code": "92618",
        "postal_code": "",
        "us_agent": {},
        "owner_operator": {
          "firm_name": "Keystone Dental Inc.",
          "owner_operator_number": "9096980",
          "official_correspondent": {
            "first_name": "Brian",
            "middle_initial": "",
            "last_name": "Lanza",
            "subaccount_company_name": "",
            "phone_number": "x-781-3283400-x"
          },
          "contact_address": {
            "address_1": "13645 Alton Pkwy Ste A",
            "address_2": "",
            "city": "Irvine",
            "state_code": "CA",
            "state_province": "",
            "iso_country_code": "US",
            "postal_code": "92618"
          }
        }
      },
      "pma_number": "",
      "k_number": "K994205",
      "products": [
        {
          "product_code": "DZE",
          "created_date": "2009-01-13",
          "owner_operator_number": "9096980",
          "exempt": "",
          "openfda": {
            "device_name": "Implant, Endosseous, Root-Form",
            "medical_specialty_description": "Dental",
            "regulation_number": "872.3640",
            "device_class": "2"
          }
        }
      ]
    }
  ]
}