Home › Optego Vision USA Inc. › Optego
Optego
Optego Vision USA Inc. · Model 98275 · UDI-DI 00360843007247
10
510(k) clearances
50
Adverse events
1
Recalls
1,429
Facilities
Description
Post-Dilation Slip-Ins, for adults, 100/box, un-sleeved
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2009-11-24 | Luxottica | The 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 docsData 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.