{
  "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": 17
    }
  },
  "results": [
    {
      "proprietary_name": [
        "MoniTorr ICP¿ External CSF Drainage and Monitoring System with Patient Line One Way Valve"
      ],
      "establishment_type": [
        "Repack or Relabel Medical Device"
      ],
      "registration": {
        "registration_number": "3008087383",
        "fei_number": "3008087383",
        "status_code": "1",
        "initial_importer_flag": "N",
        "reg_expiry_date_year": "2026",
        "name": "GEODIS",
        "address_line_1": "450 Lillard Drive",
        "address_line_2": "",
        "city": "Sparks",
        "state_code": "NV",
        "iso_country_code": "US",
        "zip_code": "89434",
        "postal_code": "",
        "us_agent": {},
        "owner_operator": {
          "firm_name": "GEODIS",
          "owner_operator_number": "10030802",
          "official_correspondent": {
            "first_name": "Christine",
            "middle_initial": "M",
            "last_name": "Vestbie",
            "subaccount_company_name": "",
            "phone_number": "x-775-3553547-x"
          },
          "contact_address": {
            "address_1": "450 Lillard Drive",
            "address_2": "",
            "city": "Sparks",
            "state_code": "NV",
            "state_province": "",
            "iso_country_code": "US",
            "postal_code": "89434"
          }
        }
      },
      "pma_number": "",
      "k_number": "K022554",
      "products": [
        {
          "product_code": "JXG",
          "created_date": "2009-11-12",
          "owner_operator_number": "10030802",
          "exempt": "",
          "openfda": {
            "device_name": "Shunt, Central Nervous System And Components",
            "medical_specialty_description": "Neurology",
            "regulation_number": "882.5550",
            "device_class": "2"
          }
        }
      ]
    }
  ]
}