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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.

8 linked reportsInjury 8
01112021-12: 1 reports for this device2022-03: 1 reports for this device2023-10: 1 reports for this device2024-01: 1 reports for this device2024-07: 1 reports for this device2024-09: 1 reports for this device2025-03: 1 reports for this device2025-04: 1 reports for this device1203100107090304
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
2023-101
2024-011
2024-071
2024-091
2025-031
2025-041
This device (reports/month)Average device in its product code (reports/device/month)
Failure-mode summaryAI-generated

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

Recall history

No recalls linked.

Individual MAUDE reports
DateReport #TypeNarrativeLink basis
2025-04-033009532798-2025-00021InjuryAvailableexact di
2025-03-143009532798-2025-00016InjuryAvailableexact di
2024-09-123009532798-2024-00096InjuryAvailableexact di
2024-07-013009532798-2024-00075InjuryAvailableexact di
2024-01-193009532798-2023-00145InjuryAvailableexact di
2023-10-243009532798-2023-00100InjuryAvailableexact di
2022-03-293009532798-2022-00074InjuryAvailableexact di
2021-12-243009532798-2021-00195InjuryAvailableexact di
Regulatory clearances

None linked.

Manufacturer compliance record

None in the loaded window.

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