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APEX Knee System
Omni Life Science, Inc. · Model KS-99162 · UDI-DI 00841690189060
10
510(k) clearances
2,280
Adverse events (2 deaths)
0
Recalls
875
Facilities
Description
TIBIAL TRIALS PAN - CONGRUENT
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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData 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.