Therapeutic Technologies, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Therapeutic Technologies, Inc. makes
Therapeutic Technologies, Inc. makes medical devices such as the FUORECAM, SPECTRASTIM TM 1000, and SPECTRASTIM 2000 MUSCLE STIMULATOR, which are types of muscle stimulators, as well as the TTI REHABILATATION GYM SYS and NEUROPATH 4000.
The company's portfolio is regulated as Class II devices and is listed in the FDA 510(k) registry, indicating that these devices have been cleared for marketing in the US, where the company is based.
Catalogue
Fuorecam Ref K093705
Regimes: 510(k) Registry: 510(k)Spectrastim Tm 1000 Ref K893964
Regimes: 510(k) Registry: 510(k)Spectrastim 2000 Muscle Stimulator Ref K900029
Regimes: 510(k) Registry: 510(k)Tti Rehabilatation Gym Sys Ref K841112
Regimes: 510(k) Registry: 510(k)Neuropath 4000 Ref K854277
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Therapeutic Technologies, Inc. have in the registry?
The registry currently lists 5 devices for Therapeutic Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Therapeutic Technologies, Inc.'s devices?
Among its 5 most recently registered devices, Therapeutic Technologies, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Therapeutic Technologies, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Therapeutic Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Therapeutic Technologies, Inc. in the registry?
The most recently registered devices listed for Therapeutic Technologies, Inc. include FUORECAM, SPECTRASTIM TM 1000, SPECTRASTIM 2000 MUSCLE STIMULATOR and TTI REHABILATATION GYM SYS.