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Revi™ Wearable Device
BLUEWIND MEDICAL LTD · Model MA-3000-1300 · UDI-DI 07290017912042
QXM
Prescription
3
510(k) clearances
31
Adverse events
0
Recalls
5
Facilities
Description
Revi Wearable Device wirelessly powers the Revi Implant and enables control of stimulation parameters.
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData 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.
