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ForceFlex

RIVERPOINT MEDICAL, LLC · Model SS654 · UDI-DI 00810020083545

PTX
0
510(k) clearances
9
Adverse events
0
Recalls
8
Facilities

Description

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.