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.
510(k) submissions have been managed by Mdi Consutants, Inc. as regulatory consultant.
1 devices