Theratronics, Inc.
Country not established
- Devices
- 9
What Theratronics, Inc. makes
Theratronics, Inc. manufactures therapeutic ultrasound devices, including the Theraplan series (V05B/TP-11 V09B, Plus versions), Theratron models (780E, 1000, 1000E, Elite), and the Theratronic Stimulator. These devices are designed for physical therapy applications, delivering controlled ultrasound energy for tissue treatment and muscle stimulation.
The company’s devices fall under FDA Class II regulation and are listed via 510(k) clearance in the United States. No additional registries or international authorisations are specified.
Catalogue
Theraplan V05B/ Tp-11 V09B Ref K940237
510(k) 510(k)Theraton 1000E Ref K964607
510(k) 510(k)Theratron 780E Ref K964606
510(k) 510(k)Theratron 1000 Ref K894165
510(k) 510(k)Theratronic Stimulator Ref K820782
510(k) 510(k)Theraplan Plus Version 1.2 Ref K970236
510(k) 510(k)Theraplan Plus Ref K954679
510(k) 510(k)Therac 25 Ref K922276
510(k) 510(k)Theratron Elite Ref K983917
510(k) 510(k)
Frequently asked questions
How many devices does Theratronics, Inc. have in the registry?
The registry currently lists 9 devices for Theratronics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Theratronics, Inc.'s devices?
Among its 9 most recently registered devices, Theratronics, Inc. has devices listed in FDA 510(k) (9 devices).
What risk classes do Theratronics, Inc.'s devices fall under?
Among its 9 most recently registered devices, the classes recorded for Theratronics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Theratronics, Inc. in the registry?
The most recently registered devices listed for Theratronics, Inc. include THERAPLAN V05B/ TP-11 V09B, THERATON 1000E, THERATRON 780E and THERATRON 1000.