FDA Device Intelligence
Home › VOLK OPTICAL INC. › Surgical Goniotomy

Surgical Goniotomy

VOLK OPTICAL INC. · Model VSGACS · UDI-DI 00811608018331

HKS
10
510(k) clearances
4
Adverse events
1
Recalls
19
Facilities

Recalls

DateFirmReason
2008-06-30Volk Optical IncThe ring of the Gonio lenses distributed was engraved as, 'G4 High Mag Gonio LNF'; however, the engraving should have read simply: 'G4 High Mag Gonio.'

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.