FDA Device Intelligence
HomeFGX INTERNATIONAL INC. › APT 9

APT 9

FGX INTERNATIONAL INC. · Model 10258931.KHL · UDI-DI 00193033407448

HQY
10
510(k) clearances
50
Adverse events
1
Recalls
1,429
Facilities

Recalls

DateFirmReason
2009-11-24LuxotticaThe lenses made for sunglass frames (Liberty Sport Slam or MaxMorpheus) do not meet the lens thickness specification established by the frame manufacturer. The lens thickness rang

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.