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Mergence™-S

ZIMMER TRABECULAR METAL TECHNOLOGY INC. · Model 96-105-00002 · UDI-DI 00889024317239

HXGODP Prescription
1
510(k) clearances
160
Adverse events (7 deaths)
0
Recalls
234
Facilities

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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.