FDA Device Intelligence
Home › Sonic Innovations, Inc. › Sonic

Sonic

Sonic Innovations, Inc. · Model 192129 · UDI-DI 05711583033259

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

Description

ET20, KIT 10 85 PB BE ENCHANT 20

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.