Osseus Fusions Systems, LLC is one of 12945 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Osseus Fusions Systems, LLC - FDA 510(k) Cleared Devices
Recent clearances: Pisces-SC Standalone Cervical Interbody System
1
Total
1
Cleared
0
Denied
Osseus Fusions Systems, LLC has 1 FDA 510(k) cleared medical devices. Based in Dallas, US.
Latest FDA clearance: Aug 2026. Active since 2026. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Osseus Fusions Systems, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Osseus Fusions Systems, LLC
1 devices