Therataxis, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Therataxis, LLC - FDA 510(k) Cleared Devices
Recent clearances: Molecular Flow Simulations
1
Total
1
Cleared
0
Denied
Therataxis, LLC has 1 FDA 510(k) cleared medical devices. Based in Baltimore, US.
Last cleared in 2021. Active since 2021. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Therataxis, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Convergent Clinical,Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Therataxis, LLC
1 devices