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BioBrace

Conmed Corporation · Model BB23X30-FA · UDI-DI 10653405988960

OWT OWY Prescription

510(k) clearances

592

Adverse events (7 deaths)

Recalls

Facilities

Description

BioBrace Reinforced Implant, Foot and Ankle, 23 x 30 mm

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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.