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Optego

Optego Vision USA Inc. · Model 9350020 · UDI-DI 00360843010063

HKT
0
510(k) clearances
0
Adverse events
0
Recalls
8
Facilities

Description

Optego Prism, 20 Diopter

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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.