Teknimed - FDA 510(k) Cleared Devices
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