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RETeval™

L K C TECHNOLOGIES, INC. · Model RETeval Complete w/o Electrodes · UDI-DI 00857901006477

HLGGWE Prescription
1
510(k) clearances
48
Adverse events
0
Recalls
31
Facilities

Description

RETeval visual electrophysiology system - Complete model w/o Electrodes

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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.