Teknimed is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Teknimed - FDA 510(k) Cleared Devices
Recent clearances: EUROSCREW NG
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.
510(k) submissions have been managed by RQMIS, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Teknimed
1 devices