{
  "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": "2026-04-13",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "third_party_flag": "N",
      "life_sustain_support_flag": "N",
      "gmp_exempt_flag": "N",
      "summary_malfunction_reporting": "Eligible",
      "product_code": "NLQ",
      "openfda": {
        "k_number": [
          "K143562",
          "K012571",
          "K043225",
          "K182272",
          "K093702",
          "K161693",
          "K170456",
          "K193563",
          "K132566",
          "K202554",
          "K124033",
          "K083060",
          "K190610",
          "K150524",
          "K250898",
          "K100537",
          "K151405",
          "K050343",
          "K241606",
          "K030598",
          "K173627",
          "K170955",
          "K111794",
          "K043358",
          "K133672",
          "K043315",
          "K233471"
        ],
        "registration_number": [
          "1650907",
          "3024021261",
          "1061124",
          "3030153385",
          "3011024991",
          "3009350690",
          "2011171",
          "3032391",
          "1417592",
          "1056128",
          "1018470",
          "2183744"
        ],
        "fei_number": [
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          "1000132435",
          "3024021261",
          "3030153385",
          "3011024991",
          "3009350690",
          "2011171",
          "3002299608",
          "1417592",
          "1000512168",
          "1018470",
          "2183744"
        ]
      },
      "review_panel": "SU",
      "medical_specialty": "",
      "device_name": "Single-Use Reprocessed Ultrasonic Surgical Instruments",
      "review_code": "",
      "unclassified_reason": "1",
      "medical_specialty_description": "Unknown",
      "device_class": "U",
      "definition": "Single-use reprocessed versions of the ultrasonic devices used in surgical procedures either for fragmentation, emulsification and aspiration of soft tissue and hard tissue or for ligation of vessels (under product code “LFL”). 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": "",
      "implant_flag": "N",
      "submission_type_id": "1"
    }
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}