{
  "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": "2026-10-26",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 3
    }
  },
  "results": [
    {
      "proprietary_name": [
        "Meduloc Intramedullary Fracture Fixation (IFF) System"
      ],
      "establishment_type": [
        "Complaint File Establishment per 21 CFR 820.198",
        "Develop Specifications But Do Not Manufacture At This Facility"
      ],
      "registration": {
        "registration_number": "3042903229",
        "fei_number": "3042903229",
        "status_code": "1",
        "initial_importer_flag": "N",
        "reg_expiry_date_year": "2026",
        "name": "MEDULOC",
        "address_line_1": "2010 Jimmy Durante Blvd Ste 200",
        "address_line_2": "",
        "city": "Del Mar",
        "state_code": "CA",
        "iso_country_code": "US",
        "zip_code": "92014",
        "postal_code": "",
        "us_agent": {},
        "owner_operator": {
          "firm_name": "Meduloc",
          "owner_operator_number": "10094686",
          "official_correspondent": {
            "first_name": "Benjamin",
            "middle_initial": "J",
            "last_name": "Arnold",
            "subaccount_company_name": "",
            "phone_number": "01-858-7201847-x"
          },
          "contact_address": {
            "address_1": "2010 Jimmy Durante Blvd",
            "address_2": "Suite 200",
            "city": "Del Mar",
            "state_code": "CA",
            "state_province": "",
            "iso_country_code": "US",
            "postal_code": "92014"
          }
        }
      },
      "pma_number": "",
      "k_number": "",
      "products": [
        {
          "product_code": "LXH",
          "created_date": "2026-01-12",
          "owner_operator_number": "10094686",
          "exempt": "",
          "openfda": {
            "device_name": "Orthopedic Manual Surgical Instrument",
            "medical_specialty_description": "Orthopedic",
            "regulation_number": "888.4540",
            "device_class": "1"
          }
        }
      ]
    }
  ]
}