Medical Device Manufacturer · FR , L'Union

Teknimed - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2023

1

Total

1

Cleared

0

Denied

Teknimed has 1 FDA 510(k) cleared medical devices. Based in L'Union, FR.

Last cleared in 2023. Active since 2023. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Teknimed Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Teknimed

1 devices

1-1 of 1

Cleared May 12, 2023

Orthopedic · 87d