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Regulatory presence across jurisdictions

The same device (matched on an identical UDI-DI) is registered in other jurisdictions. EU coverage (EUDAMED) is still phasing in — absence here does not mean a device is not marketed there.

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.

9 linked reportsInjury 8Malfunction 1
11222021-03: 1 reports for this device2021-05: 1 reports for this device2022-01: 1 reports for this device2022-03: 2 reports for this device2023-10: 1 reports for this device2025-04: 1 reports for this device2025-07: 1 reports for this device2025-09: 1 reports for this device0305010310040709
Monthly adverse-event reports for this device versus the product-code average.
MonthThis device (reports)Product-code average (reports per device)
2021-031
2021-051
2022-011
2022-032
2023-101
2025-041
2025-071
2025-091
This device (reports/month)Average device in its product code (reports/device/month)
Failure-mode summaryAI-generated

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

Recall history

No recalls linked.

Individual MAUDE reports
DateReport #TypeNarrativeLink basis
2025-09-193014128390-2025-00054InjuryAvailableexact di
2025-07-153014128390-2025-00044InjuryAvailableexact di
2025-04-303014128390-2025-00017MalfunctionAvailableexact di
2023-10-173014128390-2023-00026InjuryAvailableexact di
2022-03-023009532798-2022-00043InjuryAvailableexact di
2022-03-023009532798-2022-00002InjuryAvailableexact di
2022-01-053014128390-2021-00078InjuryAvailableexact di
2021-05-103009532798-2021-00058InjuryAvailableexact di
2021-03-313009532798-2021-00037InjuryAvailableexact di
Regulatory clearances

None linked.

Manufacturer compliance record

None in the loaded window.

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