ExacTrac Dynamic (2.0.2); ExacTrac Dynamic Surface
Jan 2026
30d
Brainlab SE
1
Total
1
Cleared
0
Denied
Brainlab SE — FDA 510(k) Submissions
Brainlab SE has submitted 1 FDA 510(k) premarket notifications since 2026, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Accelerator, Linear, Medical . Use the specialty filter in the sidebar to narrow results.
1 devices