{
  "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": 5
    }
  },
  "results": [
    {
      "proprietary_name": [
        "InterX500 Flexible Array Electrode"
      ],
      "establishment_type": [
        "Manufacture Medical Device for Another Party (Contract Manufacturer)"
      ],
      "registration": {
        "registration_number": "3008312728",
        "fei_number": "3008312728",
        "status_code": "1",
        "initial_importer_flag": "N",
        "reg_expiry_date_year": "2026",
        "name": "MORGAN NEWTON COMPANY",
        "address_line_1": "3401 Wynwood Drive",
        "address_line_2": "",
        "city": "Plano",
        "state_code": "TX",
        "iso_country_code": "US",
        "zip_code": "75074",
        "postal_code": "",
        "us_agent": {},
        "owner_operator": {
          "firm_name": "Morgan Newton Company",
          "owner_operator_number": "10059741",
          "official_correspondent": {
            "first_name": "Todd",
            "middle_initial": "",
            "last_name": "Kingrey",
            "subaccount_company_name": "",
            "phone_number": "x-972-2128080-x"
          },
          "contact_address": {
            "address_1": "3401 Wynwood Drive",
            "address_2": "",
            "city": "Plano",
            "state_code": "TX",
            "state_province": "",
            "iso_country_code": "US",
            "postal_code": "75074"
          }
        }
      },
      "pma_number": "",
      "k_number": "",
      "products": [
        {
          "product_code": "GXY",
          "created_date": "2020-04-03",
          "owner_operator_number": "10059741",
          "exempt": "",
          "openfda": {
            "device_name": "Electrode, Cutaneous",
            "medical_specialty_description": "Neurology",
            "regulation_number": "882.1320",
            "device_class": "2"
          }
        }
      ]
    }
  ]
}