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Tissue-Tek® Lab Aid®

SAKURA FINETEK U.S.A., INC. · Model 4013 · UDI-DI 08720177655620

NNK

510(k) clearances

Adverse events

Recalls

188

Facilities

Description

Top Panel, Beige

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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.