{
  "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": "2026-06-01",
    "results": {
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      "third_party_flag": "N",
      "city": "Hunt Valley",
      "advisory_committee_description": "General, Plastic Surgery",
      "address_1": "303 International Cir., Suite 190",
      "address_2": "",
      "statement_or_summary": "Summary",
      "product_code": "KKY",
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        "device_name": "Material, Polytetrafluoroethylene Vitreous Carbon, For Maxillofacial Reconstruction",
        "medical_specialty_description": "General, Plastic Surgery",
        "regulation_number": "878.3500",
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      "applicant": "Longeviti Neuro Solutions, LLC",
      "decision_date": "2021-07-15",
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}