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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.

2 linked reportsOther 2
11222019-07: 0 reports for this device; peer average 1/device2021-12: 0 reports for this device; peer average 1/device2025-09: 2 reports for this device; peer average 2/device2026-04: 0 reports for this device; peer average 1/device2026-05: 0 reports for this device; peer average 1/device2026-06: 0 reports for this device; peer average 1/device071209040506
Monthly adverse-event reports for this device versus the product-code average.
MonthThis device (reports)Product-code average (reports per device)
2019-0701
2021-1201
2025-0922
2026-0401
2026-0501
2026-0601
This device (reports/month)Average device in ISD (reports/device/month)
Failure-mode summaryAI-generated

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

Recall history

No recalls linked.

Individual MAUDE reports
DateReport #TypeNarrativeLink basis
2025-09-15MW5176073OtherAvailablemodel number
2025-09-15MW5176074OtherAvailablemodel number
Regulatory clearances

    Predicate lineage

    K080545

    Cited as predicate by: K140086, K143512, K181077, K192952, K233987

    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

    None in the loaded window.

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