Medical Device Manufacturer · US , Cordova , TN

Theramicro - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2025

Total

Cleared

Denied

Theramicro has 4 FDA 510(k) cleared medical devices. Based in Cordova, US.

Latest FDA clearance: Aug 2026. Active since 2025. Primary specialty: Orthopedic.

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

Theramicro is one of 16135 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Theramicro

4 devices

1-4 of 4