{
  "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": "2026-11-02",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "third_party_flag": "Y",
      "life_sustain_support_flag": "N",
      "gmp_exempt_flag": "N",
      "summary_malfunction_reporting": "Eligible",
      "product_code": "NQS",
      "openfda": {},
      "review_panel": "DE",
      "medical_specialty": "DE",
      "device_name": "Bracket, Metal, Orthodontic, Reprocessed",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "Dental",
      "device_class": "1",
      "definition": "Intended for use in orthodontic treatment.  The device is affixed to a tooth so that pressure can be exerted on the teeth. Reprocessing validation data for this device type must be included in a 510(k) submission. (70 FR 56911, available at https://www.govinfo.gov/content/pkg/FR-2005-09-29/pdf/05-19510.pdf).",
      "regulation_number": "872.5410",
      "implant_flag": "N",
      "submission_type_id": "1"
    }
  ]
}