Techfit Digital Surgery, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Techfit Digital Surgery, Inc. - FDA 510(k) Cleared Devices
Recent clearances: TECHFIT Patient-Specific Cranial System, TECHFIT DISRP® System, TECHFIT Diagnostic Models
4
Total
4
Cleared
0
Denied
Techfit Digital Surgery, Inc. has 4 FDA 510(k) cleared medical devices. Based in Daytona Beach, US.
Latest FDA clearance: Oct 2025. Active since 2022.
Browse the FDA 510(k) cleared devices submitted by Techfit Digital Surgery, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Techfit Digital Surgery, Inc.
4 devices