Techfit Digital Surgery is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Techfit Digital Surgery - FDA 510(k) Cleared Devices
Recent clearances: TECHFIT DISRP® System
1
Total
1
Cleared
0
Denied
Techfit Digital Surgery has 1 FDA 510(k) cleared medical devices. Based in Daytona Beach, US.
Last cleared in 2023. Active since 2023. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Techfit Digital Surgery Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Techfit Digital Surgery
1 devices