Naox Technologies Sas is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Naox Technologies Sas - FDA 510(k) Cleared Devices
Recent clearances: NX01 (NX01)
1
Total
1
Cleared
0
Denied
Naox Technologies Sas has 1 FDA 510(k) cleared medical devices. Based in Paris, FR.
Latest FDA clearance: Nov 2025. Active since 2025. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Naox Technologies Sas Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Naox Technologies Sas
1 devices