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Revi™ Implant

BLUEWIND MEDICAL LTD · Model MA-1007-1600 · UDI-DI 07290017912097

QXM
3
510(k) clearances
33
Adverse events
0
Recalls
5
Facilities

Description

Implantable, wireless, battery-less neurostimulation component of the Revi Peripheral Nerve Stimulation System

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.