Adaptix Ortho350
Nov 2025
122d
Adaptix Limited
1
Total
1
Cleared
0
Denied
Adaptix Limited — FDA 510(k) Submissions
Adaptix Limited has submitted 1 FDA 510(k) premarket notifications since 2025, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include System, X-ray, Tomographic . Use the specialty filter in the sidebar to narrow results.
1 devices