{
  "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": 2
    }
  },
  "results": [
    {
      "proprietary_name": [
        "WAVi Headset and WAVi eSoc Single Use Electrode Contacts"
      ],
      "establishment_type": [
        "Manufacture Medical Device"
      ],
      "registration": {
        "registration_number": "3013757456",
        "fei_number": "3013757456",
        "status_code": "1",
        "initial_importer_flag": "N",
        "reg_expiry_date_year": "2026",
        "name": "WAVI CO",
        "address_line_1": "3957 N. Steele St.",
        "address_line_2": "suite 1293",
        "city": "Denver",
        "state_code": "CO",
        "iso_country_code": "US",
        "zip_code": "80205",
        "postal_code": "",
        "us_agent": {},
        "owner_operator": {
          "firm_name": "WAVi Co",
          "owner_operator_number": "10055380",
          "official_correspondent": {
            "first_name": "David",
            "middle_initial": "",
            "last_name": "Oakley",
            "subaccount_company_name": "",
            "phone_number": "1-720-2036970-x"
          },
          "contact_address": {
            "address_1": "3857 steele st suite 1293",
            "address_2": "",
            "city": "Denver",
            "state_code": "CO",
            "state_province": "",
            "iso_country_code": "US",
            "postal_code": "80205"
          }
        }
      },
      "pma_number": "",
      "k_number": "K162460",
      "products": [
        {
          "product_code": "GXY",
          "created_date": "2017-07-17",
          "owner_operator_number": "10055380",
          "exempt": "",
          "openfda": {
            "device_name": "Electrode, Cutaneous",
            "medical_specialty_description": "Neurology",
            "regulation_number": "882.1320",
            "device_class": "2"
          }
        }
      ]
    }
  ]
}