Geto2, Inc.
Country not established
- Devices
- 1
What Geto2, Inc. makes
Geto2, Inc. manufactures portable oxygen therapy systems, including the O2-IN-A-BOX, designed for delivering concentrated oxygen to patients in various settings.
The company’s products are regulated as Class II medical devices under FDA 510(k) clearance requirements and are listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
O2-In-A-Box, O2-In-A-Box Ref K102750
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Geto2, Inc. have in the registry?
The registry currently lists 1 device for Geto2, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Geto2, Inc.'s devices?
Among its 1 most recently registered device, Geto2, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Geto2, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Geto2, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Geto2, Inc. in the registry?
The most recently registered devices listed for Geto2, Inc. include O2-IN-A-BOX, O2-IN-A-BOX.