Technoflex Sas. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Technoflex Sas. has 1 FDA 510(k) cleared medical devices. Based in Bidart, FR.
Latest FDA clearance: Apr 2025. Active since 2025. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Technoflex Sas. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Technoflex Sas.
1 devices