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Celadia

Biowound Solutions, Inc. · Model SS074044O-18 · UDI-DI 00850072068787

MDA
10
510(k) clearances
51
Adverse events (1 deaths)
0
Recalls
190
Facilities

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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.