Teknimed Sas is one of 26109 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Teknimed Sas - FDA 510(k) Cleared Devices
Recent clearances: GENTAFIX® (1, 3, 3MV), HIGH V+, COHESION BONE CEMENT
3
Total
3
Cleared
0
Denied
Teknimed Sas has 3 FDA 510(k) cleared medical devices. Based in Round Rock, US.
Latest FDA clearance: Dec 2024. Active since 2011. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Teknimed Sas Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by The OrthoMedix Group, Inc. and RQMIS, Inc..
FDA 510(k) Regulatory Record - Teknimed Sas
3 devices