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WoundSeal®

BIOLIFE, L.L.C. · Model WSO310ZC · UDI-DI 00834061000477

QSY Prescription
2
510(k) clearances
19
Adverse events (5 deaths)
0
Recalls
117
Facilities

Description

WoundSeal® Powder

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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.