{
  "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": {
      "skip": 0,
      "limit": 1,
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    }
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  "results": [
    {
      "third_party_flag": "N",
      "life_sustain_support_flag": "N",
      "gmp_exempt_flag": "N",
      "summary_malfunction_reporting": "Eligible",
      "product_code": "ORY",
      "openfda": {
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          "K103179",
          "K111179",
          "K121440",
          "K121814",
          "K101060",
          "K183310",
          "K201238",
          "K213159",
          "K133680"
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          "3013564228",
          "3008792120",
          "2950160"
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      "review_panel": "DE",
      "medical_specialty": "DE",
      "device_name": "Tongue Suspension System",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "Dental",
      "device_class": "2",
      "definition": "Intended to be used for anterior advancement of the tongue base by means of a bone screw threaded with a suture.  It is indicated for the treatment of obstructive sleep apnea (OSA) and/or snoring.",
      "regulation_number": "872.5570",
      "implant_flag": "Y",
      "submission_type_id": "1"
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}