Mwi, Inc.
Country not established
- Devices
- 1
What Mwi, Inc. makes
Mwi, Inc. manufactures the EXCELL 22, a medical device designed for surgical procedures, likely related to orthopedic or spinal applications given the naming convention.
The EXCELL 22 is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Excell 22 Ref K991539
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mwi, Inc. have in the registry?
The registry currently lists 1 device for Mwi, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mwi, Inc.'s devices?
Among its 1 most recently registered device, Mwi, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Mwi, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Mwi, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mwi, Inc. in the registry?
The most recently registered devices listed for Mwi, Inc. include EXCELL 22.