Skip to content
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.

3 linked reportsInjury 3
24572019-07: 0 reports for this device; peer average 1/device2021-02: 0 reports for this device; peer average 7/device2023-03: 0 reports for this device; peer average 1/device2024-06: 0 reports for this device; peer average 2/device2024-11: 0 reports for this device; peer average 1/device2025-10: 0 reports for this device; peer average 2/device2026-03: 3 reports for this device; peer average 3/device07020306111003
Monthly adverse-event reports for this device versus the product-code average.
MonthThis device (reports)Product-code average (reports per device)
2019-0701
2021-0207
2023-0301
2024-0602
2024-1101
2025-1002
2026-0333
This device (reports/month)Average device in DHB (reports/device/month)
Failure-mode summaryAI-generated

3 linked report narratives available — no AI summary generated yet.

Recall history

No recalls linked.

Individual MAUDE reports
DateReport #TypeNarrativeLink basis
2026-03-203004973408-2026-00001InjuryAvailablecatalog number

Showing the most recent 1 of 3 linked reports.

Regulatory clearances

    Predicate lineage

    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
    2013-11-21NAINo action indicatedPhadia GmbH0
    2011-08-18NAINo action indicatedPhadia Ab0
    2011-08-18NAINo action indicatedPhadia Ab0
    Similar devices
    Select up to two to place side-by-side with this device.