Spinal Resources, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Spinal Resources, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Swedge™ Pedicle Screw Fixation System Bezier Rod, Swedge™ Pedicle Screw Fixation System
4
Total
4
Cleared
0
Denied
Spinal Resources, Inc. has 4 FDA 510(k) cleared medical devices. Based in Indian Harbour Beach, US.
Latest FDA clearance: Jan 2026. Active since 2016. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Spinal Resources, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by MRC Global, LLC and Applied Technical Services (Empirical Technologies).
FDA 510(k) Regulatory Record - Spinal Resources, Inc.
4 devices