Kelyniam Global, Inc. Receives FDA Clearance for Innovative Fusion™ BCP-PEEK Implant
This 510(k) clearance marks the first time the FDA has approved this material for use in cranial and craniofacial implants, representing a significant milestone in implant technology. The Fusion™ BCP-PEEK implant is the first totally new implant launched in the cranial and craniofacial market in 8 years.
"Kelyniam's achievement as the first company in the
Designed for custom applications , the Fusion™ BCP-PEEK material meets critical neurosurgery needs where precise, patient-specific solutions are essential for treating traumatic injuries, defects from tumor resections, or congenital anomalies. As with Kelyniam's PEEK implants, Fusion™ BCP-PEEK custom implants can be designed, manufactured and shipped to surgeons within 24-48 hours, ensuring timely care for patients in need.
About Kelyniam Global, Inc. Kelyniam Global, Inc. specializes in rapidly producing custom cranial and craniofacial implants using biocompatible materials. By partnering with neurosurgeons worldwide, the company delivers high-quality, patient-specific solutions with a quick turnaround time. Dedicated to innovation in regenerative medicine, Kelyniam continues to enhance neurosurgical care. For more information, visit www.kelyniam.com .
Forward-Looking Statements This press release contains forward-looking statements under Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934. These statements involve risks and uncertainties that may cause actual results to differ from projections. Investors should not place undue reliance on these forward-looking statements.
View original content:https://www.prnewswire.com/news-releases/kelyniam-global-inc-receives-fda-clearance-for-innovative-fusion-bcp-peek-implant-302560687.html
SOURCE Kelyniam Global Inc
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