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HomeOCULUS Optikgeräte Gesellschaft mit beschränkter Haftung › GONIO ready® 200 for f=200

GONIO ready® 200 for f=200

OCULUS Optikgeräte Gesellschaft mit beschränkter Haftung · Model 10008422 · UDI-DI 04049584034465

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

Description

GONIO ready® 200 for f=200

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.'

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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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.