FDA Device Intelligence
Home › Oticon A/S › HHM

HHM

Oticon A/S · Model 193284 · UDI-DI 05707131340993

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

Description

G200, BTE 13 2.4G 85 C090 HHM

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.