The Jenex Corporation
Country not established
- Devices
- 1
What The Jenex Corporation makes
The Jenex Corporation manufactures THERAPIK, a Class II medical device designed for therapeutic applications, though specific use cases are not detailed.
THERAPIK is regulated under the FDA’s 510(k) pathway as a Class II device and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Therapik Ref K964397
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does The Jenex Corporation have in the registry?
The registry currently lists 1 device for The Jenex Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list The Jenex Corporation's devices?
Among its 1 most recently registered device, The Jenex Corporation has devices listed in FDA 510(k) (1 device).
What risk classes do The Jenex Corporation's devices fall under?
Among its 1 most recently registered device, the classes recorded for The Jenex Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from The Jenex Corporation in the registry?
The most recently registered devices listed for The Jenex Corporation include THERAPIK.