Therasigma, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Therasigma, LLC - FDA 510(k) Cleared Devices
Recent clearances: ETD4000, ETD Family of Electrotherapy Devices
2
Total
2
Cleared
0
Denied
Therasigma, LLC has 2 FDA 510(k) cleared medical devices. Based in Washougal, US.
Last cleared in 2021. Active since 2020. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Therasigma, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Accelerated Device Approval Services as regulatory consultant.
FDA 510(k) Regulatory Record - Therasigma, LLC
2 devices