Wjo, Inc.
Country not established
- Devices
- 1
What Wjo, Inc. makes
Wjo, Inc. manufactures the Hyperox 101, a medical device designed for oxygen therapy delivery, likely intended for clinical or home use to provide controlled oxygen administration.
The Hyperox 101 is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Hyperox 101 Ref K053498
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Wjo, Inc. have in the registry?
The registry currently lists 1 device for Wjo, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Wjo, Inc.'s devices?
Among its 1 most recently registered device, Wjo, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Wjo, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Wjo, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Wjo, Inc. in the registry?
The most recently registered devices listed for Wjo, Inc. include HYPEROX 101.