{
  "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": "2026-07-27",
    "results": {
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  "results": [
    {
      "third_party_flag": "N",
      "city": "Dublin 8",
      "advisory_committee_description": "Ear, Nose, Throat",
      "address_1": "Rainsford St.",
      "address_2": "",
      "statement_or_summary": "",
      "product_code": "QVN",
      "openfda": {
        "device_name": "Combined Acoustic And Electrical External Stimulation Device For The Relief Of Tinnitus",
        "medical_specialty_description": "Ear, Nose, Throat",
        "regulation_number": "874.3410",
        "device_class": "2",
        "registration_number": [
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          "3018030059",
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      "zip_code": "D08 R2YP",
      "applicant": "Neuromod Devices Limited",
      "decision_date": "2023-03-06",
      "decision_code": "DENG",
      "country_code": "IE",
      "device_name": "Lenire Tinnitus Treatment Device",
      "advisory_committee": "EN",
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      "expedited_review_flag": "",
      "k_number": "DEN210033",
      "state": "",
      "date_received": "2021-08-18",
      "review_advisory_committee": "EN",
      "postal_code": "D08 R2YP",
      "decision_description": "Unknown",
      "clearance_type": "Direct"
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}