FDA Device Intelligence
Home › FGX INTERNATIONAL INC. › FRYE & CO

FRYE & CO

FGX INTERNATIONAL INC. · Model 5013179-000.LTS · UDI-DI 00193033474563

HOI
10
510(k) clearances
26
Adverse events
0
Recalls
677
Facilities

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.