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EXULT Knee Replacement System

Corentec Co., Ltd · Model KA.CPM.0001 · UDI-DI 08800017282503

KTZ Prescription

510(k) clearances

Adverse events

Recalls

194

Facilities

Description

Patella Calipers

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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.