FDA Device Intelligence
Home › BIOLIFE, L.L.C. › WoundSeal®

WoundSeal®

BIOLIFE, L.L.C. · Model DWS001 · UDI-DI 00834061000255

QSY Prescription
1
510(k) clearances
19
Adverse events (5 deaths)
0
Recalls
118
Facilities

Description

WoundSeal® Disc - Advanced

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
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.