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Kelyniam CSI

KELYNIAM GLOBAL, INC. · Model PEEK-IM1002 · UDI-DI 00817580028511

GXN Prescription
1
510(k) clearances
827
Adverse events (2 deaths)
0
Recalls
49
Facilities

Description

PEEK Customized Cranial Implant, Medium CSI011320-ME1

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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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.