Pace Surgical is one of 16117 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pace Surgical - FDA 510(k) Cleared Devices
Recent clearances: Tempo Plating System, Ultra™ Compression Screw System
2
Total
2
Cleared
0
Denied
Pace Surgical has 2 FDA 510(k) cleared medical devices. Based in Malvern, US.
Latest FDA clearance: Sep 2026. Active since 2025. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Pace Surgical Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by MRC Global and MRC Global, LLC.
FDA 510(k) Regulatory Record - Pace Surgical
2 devices