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MAGNIVISION

FGX INTERNATIONAL INC. · Model 5011736-200.MCV · UDI-DI 00193033337110

HOI
10
510(k) clearances
26
Adverse events
0
Recalls
677
Facilities

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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.