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DemeLENE

Demetech Corporation · Model PM290026B1P · UDI-DI 10652927290919

GAW Prescription
1
510(k) clearances
20,028
Adverse events (226 deaths)
0
Recalls
111
Facilities

Description

Synthetic (polypropylene), Non Absorbable Suture

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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.