Medical Device Manufacturer · US , Daytona Beach , FL

Techfit Digital Surgery, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2022
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.

FDA 510(k) cleared devices by Techfit Digital Surgery, Inc.

4 devices
1-4 of 4
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