Foundation Surgical Group, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Foundation Surgical Group, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Foundation Surgical Navigated Lateral Disc Prep Instruments, Vertiwedge® Intraosseous System, Interwedge® Standalone Lateral
3
Total
3
Cleared
0
Denied
Foundation Surgical Group, Inc. has 3 FDA 510(k) cleared medical devices. Based in Scottsdale, US.
Latest FDA clearance: Apr 2026. Active since 2024. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Foundation Surgical Group, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Empirical Technologies and Applied Technical Services (Empirical Technologies).
FDA 510(k) Regulatory Record - Foundation Surgical Group, Inc.
3 devices