Thermosurgery Technologies, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 2027460
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
What Thermosurgery Technologies, Inc. makes
Thermosurgery Technologies, Inc. makes the Thermomed 1.8 and TTI Thermomed Model 1.8 Instrument, which are surgical devices used for thermal tissue treatment.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Thermomed 1.8 Ref K063748
Regimes: 510(k) Registry: 510(k)Tti Thermomed Model 1.8 Instrument Ref K021117
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 2027460
- Address
- 236 S Mulberry Ste 107, Mesa, AZ, 85202
Frequently asked questions
How many devices does THERMOSURGERY TECHNOLOGIES, INC. have in the registry?
The registry currently lists 2 devices for THERMOSURGERY TECHNOLOGIES, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list THERMOSURGERY TECHNOLOGIES, INC.'s devices?
Among its 2 most recently registered devices, THERMOSURGERY TECHNOLOGIES, INC. has devices listed in FDA 510(k) (2 devices).
What risk classes do THERMOSURGERY TECHNOLOGIES, INC.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for THERMOSURGERY TECHNOLOGIES, INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from THERMOSURGERY TECHNOLOGIES, INC. in the registry?
The most recently registered devices listed for THERMOSURGERY TECHNOLOGIES, INC. include THERMOMED 1.8 and TTI THERMOMED MODEL 1.8 INSTRUMENT.