Jennifermaxx, Inc.
Country not established
- Devices
- 1
What Jennifermaxx, Inc. makes
Jennifermaxx, Inc. manufactures the THERMALIGHT 2000, a medical device designed for thermal imaging applications in clinical settings.
The THERMALIGHT 2000 is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Thermalight 2000 Ref K992630
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Jennifermaxx, Inc. have in the registry?
The registry currently lists 1 device for Jennifermaxx, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Jennifermaxx, Inc.'s devices?
Among its 1 most recently registered device, Jennifermaxx, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Jennifermaxx, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Jennifermaxx, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Jennifermaxx, Inc. in the registry?
The most recently registered devices listed for Jennifermaxx, Inc. include THERMALIGHT 2000.