FDA Device Intelligence
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Tissue-Tek® Lab Aid® Ultra™ II

SAKURA FINETEK U.S.A., INC. · Model 3990 · UDI-DI 08720177655583

NNK
0
510(k) clearances
18
Adverse events
0
Recalls
188
Facilities

Description

Cabinet

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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.