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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.

4 linked reportsMalfunction 3Injury 1
01112022-10: 1 reports for this device2023-03: 1 reports for this device2023-07: 1 reports for this device2025-08: 1 reports for this device10030708
Monthly adverse-event reports for this device versus the product-code average.
MonthThis device (reports)Product-code average (reports per device)
2022-101
2023-031
2023-071
2025-081
This device (reports/month)Average device in its product code (reports/device/month)
Failure-mode summaryAI-generated

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

Recall history

No recalls linked.

Individual MAUDE reports
DateReport #TypeNarrativeLink basis
2025-08-213006493760-2025-00004MalfunctionAvailableexact di
2023-07-283006493760-2023-00002InjuryAvailableexact di
2023-03-073006493760-2023-00001MalfunctionAvailableexact di
2022-10-283006493760-2022-00002MalfunctionAvailableexact di
Regulatory clearances

None linked.

Manufacturer compliance record

None in the loaded window.

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