Greene & Kellogg, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Greene & Kellogg, Inc. makes
Greene & Kellogg, Inc. manufactures medical oxygen-rich air supply devices, including portable and stationary models like the RXO2, 52 Bunn, and HI-FLO2 systems, as well as oxygen concentrators such as the Bunn Micro. These products are designed to deliver enriched oxygen for therapeutic use in clinical and home settings.
The company’s devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. They are based in the United States and comply with U.S. medical device authorization requirements.
Catalogue
Model RXO2 Oxygen Rich Air Supply Ref K811155
Regimes: 510(k) Registry: 510(k)Model 52 Bunn Dry Air Supply Ref K800534
Regimes: 510(k) Registry: 510(k)Model Hi-FLO2 Oxygen Rich Air Supply Ref K830046
Regimes: 510(k) Registry: 510(k)Bunn Micro Oxygen Concentrator Ref K833495
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Greene & Kellogg, Inc. have in the registry?
The registry currently lists 4 devices for Greene & Kellogg, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Greene & Kellogg, Inc.'s devices?
Among its 4 most recently registered devices, Greene & Kellogg, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Greene & Kellogg, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Greene & Kellogg, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Greene & Kellogg, Inc. in the registry?
The most recently registered devices listed for Greene & Kellogg, Inc. include MODEL RXO2 OXYGEN RICH AIR SUPPLY, MODEL 52 BUNN DRY AIR SUPPLY, MODEL HI-FLO2 OXYGEN RICH AIR SUPPLY and BUNN MICRO OXYGEN CONCENTRATOR.