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Maxima

HENRY SCHEIN, INC. · Model 1127258 · UDI-DI 10304040001230

NBY Prescription
10
510(k) clearances
27
Adverse events
0
Recalls
34
Facilities

Description

Maxima Suture PTFE

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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.