Therasigma, LLC
United StatesFDA applicant, unverified
- Devices
- 2
What Therasigma, LLC makes
Therasigma, LLC manufactures the ETD Family of Electrotherapy Devices, including the ETD4000, which are designed for therapeutic electrical stimulation applications.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
ETD Family of Electrotherapy Devices Ref K201958
Regimes: 510(k) Registry: 510(k)ETD4000 Ref K202725
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Therasigma, LLC have in the registry?
The registry currently lists 2 devices for Therasigma, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Therasigma, LLC's devices?
Among its 2 most recently registered devices, Therasigma, LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do Therasigma, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Therasigma, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Therasigma, LLC in the registry?
The most recently registered devices listed for Therasigma, LLC include ETD Family of Electrotherapy Devices and ETD4000.