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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.

  • United StatesAVANTI10705032010283
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.

41 linked reportsMalfunction 40Injury 1
71522292020-12: 1 reports for this device2021-11: 1 reports for this device2022-07: 1 reports for this device2023-03: 1 reports for this device2024-07: 1 reports for this device2024-11: 1 reports for this device2025-02: 1 reports for this device2025-03: 1 reports for this device2025-07: 1 reports for this device2025-09: 1 reports for this device2026-01: 1 reports for this device2026-05: 29 reports for this device2026-06: 1 reports for this device12110703071102030709010506
Monthly adverse-event reports for this device versus the product-code average.
MonthThis device (reports)Product-code average (reports per device)
2020-121
2021-111
2022-071
2023-031
2024-071
2024-111
2025-021
2025-031
2025-071
2025-091
2026-011
2026-0529
2026-061
This device (reports/month)Average device in its product code (reports/device/month)
Failure-mode summaryAI-generated

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

Recall history

No recalls linked.

Individual MAUDE reports
DateReport #TypeNarrativeLink basis
2026-06-109616099-2026-00839MalfunctionAvailableexact di
2026-05-049616099-2026-00641MalfunctionAvailableexact di
2026-05-049616099-2026-00634MalfunctionAvailableexact di
2026-05-049616099-2026-00624MalfunctionAvailableexact di
2026-05-049616099-2026-00633MalfunctionAvailableexact di
2026-05-049616099-2026-00628MalfunctionAvailableexact di
2026-05-049616099-2026-00630MalfunctionAvailableexact di
2026-05-049616099-2026-00618MalfunctionAvailableexact di
2026-05-049616099-2026-00643MalfunctionAvailableexact di
2026-05-049616099-2026-00642MalfunctionAvailableexact di
2026-05-049616099-2026-00632MalfunctionAvailableexact di
2026-05-049616099-2026-00622MalfunctionAvailableexact di
2026-05-049616099-2026-00649MalfunctionAvailableexact di
2026-05-049616099-2026-00645MalfunctionAvailableexact di
2026-05-049616099-2026-00639MalfunctionAvailableexact di
Showing 115 of 41
Regulatory clearances

None linked.

Manufacturer compliance record
DateTypeOutcomeFacilityCitations
2022-06-29VAIVoluntary action indicatedCordis US Corp0
2022-06-29VAIVoluntary action indicatedCordis US Corp0
2018-01-12VAIVoluntary action indicatedCordis US Corp1
2018-01-12VAIVoluntary action indicatedCordis US Corp1
2017-09-15VAIVoluntary action indicatedAccessClosure, Inc., A Cardinal Health Company1
2016-07-06NAINo action indicatedCordis US Corp0
2016-07-06NAINo action indicatedCordis US Corp0
2016-03-31NAINo action indicatedCordis US Corp0
2016-03-31NAINo action indicatedCordis US Corp0
2016-02-12VAIVoluntary action indicatedCardinal Health Mexico 244 S de RL de CV3
2016-02-01NAINo action indicatedAccessClosure, Inc., A Cardinal Health Company0
2015-05-08NAINo action indicatedCordis US Corp0
2015-05-08NAINo action indicatedCordis US Corp0
2014-08-05VAIVoluntary action indicatedAccessClosure, Inc., A Cardinal Health Company3
2014-04-03NAINo action indicatedCardinal Health Mexico 244 S de RL de CV0
2014-01-30NAINo action indicatedCordis US Corp0
2014-01-30NAINo action indicatedCordis US Corp0
2013-12-18NAINo action indicatedCordis US Corp0
2013-12-18NAINo action indicatedCordis US Corp0
2012-07-03NAINo action indicatedCordis US Corp0
2011-02-16WLWarning LetterCordis LLC
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