Xelite Biomed , Ltd. is one of 203 FDA 510(k) medical device manufacturers from Taiwan in the dataset, ranked by real submission volume.
Xelite Biomed , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: XeliteMed SuperM-Fix Spinal Bone Cement, XeliteMed VertehighFix High Viscosity Spinal Bone Cement System, XeliteMed VertehighFix High Viscosity Spinal Bone Cement
3
Total
3
Cleared
0
Denied
Xelite Biomed , Ltd. has 3 FDA 510(k) cleared medical devices. Based in New Taipei City, TW.
Latest FDA clearance: Jan 2026. Active since 2024. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Xelite Biomed , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Xelite Biomed , Ltd.
3 devices