{
  "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": "2026-09-07",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 48
    }
  },
  "results": [
    {
      "proprietary_name": [
        "MODIFICATION TO THE MAESTRO SYSTEM"
      ],
      "establishment_type": [
        "Manufacture Medical Device for Another Party (Contract Manufacturer)"
      ],
      "registration": {
        "registration_number": "3017980266",
        "fei_number": "3017980266",
        "status_code": "1",
        "initial_importer_flag": "N",
        "reg_expiry_date_year": "2026",
        "name": "Precision One Medical",
        "address_line_1": "2100 Riverchase Ctr Ste 106",
        "address_line_2": "",
        "city": "Hoover",
        "state_code": "AL",
        "iso_country_code": "US",
        "zip_code": "35244",
        "postal_code": "",
        "us_agent": {},
        "owner_operator": {
          "firm_name": "Precision One Medical",
          "owner_operator_number": "10042281",
          "official_correspondent": {
            "first_name": "Amose",
            "middle_initial": "",
            "last_name": "Kim",
            "subaccount_company_name": "",
            "phone_number": "001-760-9457966-5213"
          },
          "contact_address": {
            "address_1": "3923 Oceanic Dr.",
            "address_2": "Suite 200",
            "city": "Oceanside",
            "state_code": "CA",
            "state_province": "",
            "iso_country_code": "US",
            "postal_code": "92056"
          }
        }
      },
      "pma_number": "",
      "k_number": "",
      "products": [
        {
          "product_code": "DZE",
          "created_date": "2021-07-01",
          "owner_operator_number": "10042281",
          "exempt": "",
          "openfda": {
            "device_name": "Implant, Endosseous, Root-Form",
            "medical_specialty_description": "Dental",
            "regulation_number": "872.3640",
            "device_class": "2"
          }
        }
      ]
    }
  ]
}