{
  "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": 1
    }
  },
  "results": [
    {
      "proprietary_name": [
        "Kinesia StimPoint",
        "KinesiaU",
        "Kinesia",
        "Kinesia 360",
        "Kinesia ProView",
        "Kinesia ONE",
        "Kinesia HomeView",
        "Kinesia ONE-C"
      ],
      "establishment_type": [
        "Manufacture Medical Device"
      ],
      "registration": {
        "registration_number": "3009134706",
        "fei_number": "3009134706",
        "status_code": "1",
        "initial_importer_flag": "N",
        "reg_expiry_date_year": "2026",
        "name": "GREAT LAKES NEUROTECHNOLOGIES INC.",
        "address_line_1": "6100 Rockside Woods Blvd.",
        "address_line_2": "Suite 415",
        "city": "Cleveland",
        "state_code": "OH",
        "iso_country_code": "US",
        "zip_code": "44131",
        "postal_code": "",
        "us_agent": {},
        "owner_operator": {
          "firm_name": "Great Lakes NeuroTechnologies Inc.",
          "owner_operator_number": "10035940",
          "official_correspondent": {
            "first_name": "Dustin",
            "middle_initial": "",
            "last_name": "Heldman",
            "subaccount_company_name": "",
            "phone_number": "x-216-4462437-x"
          },
          "contact_address": {
            "address_1": "6100 Rockside Woods Blvd.",
            "address_2": "Suite 415",
            "city": "Cleveland",
            "state_code": "OH",
            "state_province": "",
            "iso_country_code": "US",
            "postal_code": "44131"
          }
        }
      },
      "pma_number": "",
      "k_number": "K063872",
      "products": [
        {
          "product_code": "GYD",
          "created_date": "2011-04-05",
          "owner_operator_number": "10035940",
          "exempt": "",
          "openfda": {
            "k_number": [
              "K063872"
            ],
            "device_name": "Transducer, Tremor",
            "medical_specialty_description": "Neurology",
            "regulation_number": "882.1950",
            "device_class": "2"
          }
        }
      ]
    }
  ]
}