Naox Technologies Sas

Naox Technologies Sas — FDA 510(k) Submissions

Naox Technologies Sas 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 Reduced- Montage Standard Electroencephalograph . Use the specialty filter in the sidebar to narrow results.