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Adverse-event reports (MAUDE)

Read this first: MAUDE report counts cannot be used to compute incidence rates or compare device safety. Reporting is incomplete, duplicated, and spikes with publicity; there is no denominator of devices in use. The peer line shows reporting volume for the average device in the same FDA product code — a reporting baseline, not a risk measure.

1 linked reportInjury 1
11222019-07: 0 reports for this device; peer average 1/device2019-09: 0 reports for this device; peer average 1/device2019-11: 0 reports for this device; peer average 1/device2021-02: 0 reports for this device; peer average 1/device2021-09: 0 reports for this device; peer average 1/device2022-05: 0 reports for this device; peer average 1.5/device2022-11: 0 reports for this device; peer average 1.5/device2022-12: 0 reports for this device; peer average 2/device2023-10: 0 reports for this device; peer average 1/device2023-11: 0 reports for this device; peer average 1/device2023-12: 0 reports for this device; peer average 1/device2024-01: 0 reports for this device; peer average 1/device2024-10: 1 reports for this device; peer average 1/device2025-02: 0 reports for this device; peer average 1/device2025-05: 0 reports for this device; peer average 1/device2025-06: 0 reports for this device; peer average 2/device2025-09: 0 reports for this device; peer average 1/device2026-05: 0 reports for this device; peer average 1/device070911020905111210111201100205060905
Monthly adverse-event reports for this device versus the product-code average.
MonthThis device (reports)Product-code average (reports per device)
2019-0701
2019-0901
2019-1101
2021-0201
2021-0901
2022-0501.5
2022-1101.5
2022-1202
2023-1001
2023-1101
2023-1201
2024-0101
2024-1011
2025-0201
2025-0501
2025-0602
2025-0901
2026-0501
This device (reports/month)Average device in JWJ (reports/device/month)
Failure-mode summaryAI-generated

1 linked report narrative available — no AI summary generated yet.

Recall history

No recalls linked.

Individual MAUDE reports
DateReport #TypeNarrativeLink basis
2024-10-293002788818-2024-00113InjuryAvailableexact di
Regulatory clearances

    Predicate lineage

    Cited as predicate by: K191525

    Lineage each submission cites, walked transitively (indented = the cited device's own predicates). Extracted from public 510(k) summary text — heuristic, and includes reference devices mentioned alongside true predicates.

    Manufacturer compliance record
    DateTypeOutcomeFacilityCitations
    2025-01-27NAINo action indicatedIntegrity Orthopaedics Inc0
    2023-05-03NAINo action indicatedCARTIHEAL, LTD0
    2021-12-09VAIVoluntary action indicatedSmith & Nephew, Inc.1
    2021-12-09VAIVoluntary action indicatedSmith & Nephew, Inc.1
    2021-10-26NAINo action indicatedSmith & Nephew Inc.0
    2021-10-26NAINo action indicatedSmith & Nephew Inc.0
    2020-02-06VAIVoluntary action indicatedBlue Belt Technologies, Inc6
    2019-10-25NAINo action indicatedTusker Medical, Inc.0
    2019-10-08VAIVoluntary action indicatedTusker Medical, Inc.3
    2018-03-30NAINo action indicatedAscension Orthopedics, Inc0
    2018-02-02NAINo action indicatedSmith & Nephew, Inc.0
    2018-02-02NAINo action indicatedSmith & Nephew, Inc.0
    2018-01-30NAINo action indicatedSmith & Nephew0
    2017-08-21NAINo action indicatedSmith & Nephew, Inc. Advanced Surgical Devices Division0
    2017-08-02VAIVoluntary action indicatedSmith & Nephew, Inc.3
    2017-08-02VAIVoluntary action indicatedSmith & Nephew, Inc.3
    2017-07-24NAINo action indicatedSmith & Nephew, Inc.0
    2017-07-24NAINo action indicatedSmith & Nephew, Inc.0
    2017-05-25NAINo action indicatedSmith & Nephew, Inc.0
    2017-05-25NAINo action indicatedSmith & Nephew, Inc.0
    2015-04-30WLWarning LetterSmith & Nephew Inc.
    2015-04-30WLWarning LetterSmith & Nephew Inc.
    2014-06-11WLWarning LetterSmith & Nephew, Inc.
    2010-09-16WLWarning LetterAscension Orthopedics, Inc
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