Geen Healthcare, Inc.
CanadaFDA applicant, unverified
- Devices
- 1
What Geen Healthcare, Inc. makes
Geen Healthcare, Inc. manufactures the GEEN MEDISOX, a medical device designed for monitoring and managing patient oxygen therapy, including precise delivery and monitoring of oxygen levels.
The GEEN MEDISOX 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
Geen Medisox Ref K981296
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Geen Healthcare, Inc. have in the registry?
The registry currently lists 1 device for Geen Healthcare, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Geen Healthcare, Inc.'s devices?
Among its 1 most recently registered device, Geen Healthcare, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Geen Healthcare, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Geen Healthcare, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Geen Healthcare, Inc. in the registry?
The most recently registered devices listed for Geen Healthcare, Inc. include GEEN MEDISOX.