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EyeMax2

MAXTEC, LLC · Model R300P01 · UDI-DI 00853061006920

FOK
5
510(k) clearances
27
Adverse events (1 deaths)
0
Recalls
28
Facilities

Description

Regular 20/pack

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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.