Wright Industries
Country not established
- Devices
- 1
What Wright Industries makes
Wright Industries manufactures the Wright 1000 Monoplace Hyperbaric System, a medical device designed for hyperbaric oxygen therapy in single-patient chambers.
The device is classified as Class II under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Wright 1000 Monoplace Hyperbaric System Ref K952545
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Wright Industries have in the registry?
The registry currently lists 1 device for Wright Industries. Devices recorded under merged duplicate company entries are counted once.
Which registries list Wright Industries's devices?
Among its 1 most recently registered device, Wright Industries has devices listed in FDA 510(k) (1 device).
What risk classes do Wright Industries's devices fall under?
Among its 1 most recently registered device, the classes recorded for Wright Industries's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Wright Industries in the registry?
The most recently registered devices listed for Wright Industries include WRIGHT 1000 MONOPLACE HYPERBARIC SYSTEM.