Techmah Medical, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Techmah Medical, LLC - FDA 510(k) Cleared Devices
Recent clearances: Smart SPACE Shoulder System, Smart SPACE Shoulder System, SmartSPACE Shoulder System
3
Total
3
Cleared
0
Denied
Techmah Medical, LLC has 3 FDA 510(k) cleared medical devices. Based in Knoxville, US.
Last cleared in 2021. Active since 2019. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Techmah Medical, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Medical Device Academy, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Techmah Medical, LLC
3 devices