Clini-Therm Corp.
Country not established
- Devices
- 2
What Clini-Therm Corp. makes
Clini-Therm Corp. manufactures medical devices for temperature monitoring and therapeutic applications, including the THERMO SENTRY 1200 (a thermal monitoring system) and the CLINI-THERM MARK I/IV (likely a hyperthermia or temperature-controlled therapy device). These products are designed for clinical use in controlled temperature environments, such as cancer treatment or patient stabilization.
The company’s portfolio includes devices classified as Class II and Class III under FDA regulations, with some products authorised via the 510(k) pathway and others through the PMA process. These devices are listed in the FDA’s regulatory databases, and the company operates from the United States.
Catalogue
Thermo Sentry 1200 Thermo-Sys-TS1200 Ref K833711
Regimes: 510(k) Registry: 510(k)Clini-Therm Mark I/Iv Ref P840015
Regimes: PMA Registry: PMA
Frequently asked questions
How many devices does Clini-Therm Corp. have in the registry?
The registry currently lists 2 devices for Clini-Therm Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Clini-Therm Corp.'s devices?
Among its 2 most recently registered devices, Clini-Therm Corp. has devices listed in FDA 510(k) (1 device) and FDA PMA (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Clini-Therm Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Clini-Therm Corp.'s devices are Class II and Class III. Each device page shows its own class and authorisation.
What are the newest devices from Clini-Therm Corp. in the registry?
The most recently registered devices listed for Clini-Therm Corp. include THERMO SENTRY 1200 THERMO-SYS-TS1200 and CLINI-THERM MARK I/IV.