FDA Device Intelligence
Home › Bernafon AG › Bernafon

Bernafon

Bernafon AG · Model 222102 · UDI-DI 05714464009657

KLWOSM Prescription
10
510(k) clearances
9
Adverse events
0
Recalls
31
Facilities

Description

AO7 MNR T R MSIL ALIGO 7 GPL

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 docs
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.