Oxlife, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 5
What Oxlife, Inc. makes
Oxlife, Inc. manufactures oxygen concentrators, including the Oxlife Excell Oxygen Concentrator and other models under the Oxlife Oxygen Concentrator line.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Oxlife Excell Oxygen Concentrators Ref K971964
510(k) 510(k)Oxlife Independence Oxygen Concentrators Ref K080082
510(k) 510(k)- 510(k) 510(k)
Oxlife Oxygen Concentrator Ref K933081
510(k) 510(k)Oxlife Oxygen Concentrators Ref K955549
510(k) 510(k)
Frequently asked questions
How many devices does Oxlife, Inc. have in the registry?
The registry currently lists 5 devices for Oxlife, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Oxlife, Inc.'s devices?
Among its 5 most recently registered devices, Oxlife, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Oxlife, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Oxlife, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Oxlife, Inc. in the registry?
The most recently registered devices listed for Oxlife, Inc. include OXLIFE EXCELL OXYGEN CONCENTRATORS, OXLIFE INDEPENDENCE OXYGEN CONCENTRATORS, OXLIFE FREEDOM FIVE OXYGEN CONCENTRATORS, MODEL KXF5 and OXLIFE OXYGEN CONCENTRATOR.