{
  "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": 2
    }
  },
  "results": [
    {
      "proprietary_name": [
        "Wrist Actigraph"
      ],
      "establishment_type": [
        "Manufacture Medical Device for Another Party (Contract Manufacturer)"
      ],
      "registration": {
        "registration_number": "3029922",
        "fei_number": "3001452666",
        "status_code": "1",
        "initial_importer_flag": "N",
        "reg_expiry_date_year": "2026",
        "name": "CONTROLTEK, INC.",
        "address_line_1": "3905 NE 112TH AVE.",
        "address_line_2": "",
        "city": "Vancouver",
        "state_code": "WA",
        "iso_country_code": "US",
        "zip_code": "98682",
        "postal_code": "",
        "us_agent": {},
        "owner_operator": {
          "firm_name": "CONTROLTEK, INC.",
          "owner_operator_number": "9023255",
          "official_correspondent": {
            "first_name": "Janine",
            "middle_initial": "R",
            "last_name": "Holder",
            "subaccount_company_name": "",
            "phone_number": "x-360-8969375-6029"
          },
          "contact_address": {
            "address_1": "3905 NE 112TH AVE.",
            "address_2": "--",
            "city": "Vancouver",
            "state_code": "WA",
            "state_province": "",
            "iso_country_code": "US",
            "postal_code": "98682"
          }
        }
      },
      "pma_number": "",
      "k_number": "",
      "products": [
        {
          "product_code": "GWQ",
          "created_date": "2014-12-08",
          "owner_operator_number": "9023255",
          "exempt": "",
          "openfda": {
            "device_name": "Full-Montage Standard Electroencephalograph",
            "medical_specialty_description": "Neurology",
            "regulation_number": "882.1400",
            "device_class": "2"
          }
        }
      ]
    }
  ]
}