Theramicro is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Theramicro - FDA 510(k) Cleared Devices
Recent clearances: TeKBrace Knotless Anchor, TekBrace Solo Soft Tissue Reinforcement Device
3
Total
3
Cleared
0
Denied
Theramicro has 3 FDA 510(k) cleared medical devices. Based in Cordova, US.
Latest FDA clearance: Jun 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.
FDA 510(k) Regulatory Record - Theramicro
3 devices