Teknimed Sas - FDA 510(k) Cleared Devices

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.

510(k) submissions have been managed by RQMIS, Inc. as regulatory consultant.