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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.

6 linked reportsInjury 6
01112021-12: 1 reports for this device2022-03: 1 reports for this device2022-04: 1 reports for this device2024-12: 1 reports for this device2025-06: 1 reports for this device2025-11: 1 reports for this device120304120611
Monthly adverse-event reports for this device versus the product-code average.
MonthThis device (reports)Product-code average (reports per device)
2021-121
2022-031
2022-041
2024-121
2025-061
2025-111
This device (reports/month)Average device in its product code (reports/device/month)
Failure-mode summaryAI-generated

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

Recall history

No recalls linked.

Individual MAUDE reports
DateReport #TypeNarrativeLink basis
2025-11-173009532798-2025-00067InjuryAvailableexact di
2025-06-093009532798-2025-00038InjuryAvailableexact di
2024-12-053014128390-2024-00066InjuryAvailableexact di
2022-04-153009532798-2022-00103InjuryAvailableexact di
2022-03-253009532798-2022-00007InjuryAvailableexact di
2021-12-103014128390-2021-00064InjuryAvailableexact di
Regulatory clearances

None linked.

Manufacturer compliance record

None in the loaded window.

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