VERAFEYE System VERAFEYE Imaging Catheter & VERAFEYE Imaging System
Mar 2025
182d
Luma Vision Limited
1
Total
1
Cleared
0
Denied
Luma Vision Limited — FDA 510(k) Submissions
Luma Vision 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 Catheter, Ultrasound, Intravascular . Use the specialty filter in the sidebar to narrow results.
1 devices