FDA Device Intelligence
Home › Oticon A/S › Oticon

Oticon

Oticon A/S · Model 150129 · UDI-DI 05707131284792

OSM Prescription
1
510(k) clearances
673
Adverse events
0
Recalls
81
Facilities

Description

H15V2, MINIRITE 312 WL DBL

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.