FDA 510(k) Applications Submitted by Kelyniam Global Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K250334 02/05/2025 Fusion Craniofacial Implant; Fusion Skull Implant Kelyniam Global Inc.
K182711 09/27/2018 Customized Craniofacial Implant (CCI), Customized Skull Implant (CSI) Kelyniam Global Inc.


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