Theratech, Inc.
Country not established
- Devices
- 5
What Theratech, Inc. makes
Theratech, Inc. manufactures interferential stimulators, including true sine wave models such as the WL-2206, WL-2206A1, WI-2206A2, and WL-2206A, designed for therapeutic electrical stimulation. Their portfolio also includes transcutaneous electrical nerve stimulation (TENS) devices, such as the TTech Model 200E, and powered muscle stimulators for rehabilitation and pain management applications.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearances. Theratech, Inc. is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Ttech Model 200E + Tens Device Ref K021436
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Powered Muscle Stimulator Ref K013768
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Theratech, Inc. have in the registry?
The registry currently lists 5 devices for Theratech, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Theratech, Inc.'s devices?
Among its 5 most recently registered devices, Theratech, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Theratech, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Theratech, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Theratech, Inc. in the registry?
The most recently registered devices listed for Theratech, Inc. include IF SERIES TRUE SINE INTERFERENTIAL STIMULATOR/MODEL: WL-2206, WELL IF, LIFE IF AND THE CUSTOMER PRIVATE BRAND, TTECH MODEL 200E + TENS DEVICE, IF TRUE SINE INTERFERENTIAL STIMULATOR / MODEL WL-2206A1 & WI-2206A2 and POWERED MUSCLE STIMULATOR.