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Optego

Optego Vision USA Inc. · Model 93450 · UDI-DI 00360843007278

HPC
10
510(k) clearances
2
Adverse events
0
Recalls
56
Facilities

Description

Standard Diagnostic Flipper Set +/-0.25 Purple +/-0.50 Green +/-0.75 Yellow +/-1.00 Red +/-1.50 Blue +/-2.00 Orange

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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.