FDA Device Intelligence
Home › ZYRIS, INC. › Isolite Mouthpiece

Isolite Mouthpiece

ZYRIS, INC. · Model AIL0250 · UDI-DI 00810032661250

EIFDYN
4
510(k) clearances
15
Adverse events (1 deaths)
0
Recalls
171
Facilities

Description

Customer Success Kit, OUS

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.