Nephosity, Inc.
Country not established
- Devices
- 1
What Nephosity, Inc. makes
Nephosity, Inc. manufactures the MOBILECT VIEWER, a device designed for imaging and analysis in nephrology, likely used for renal diagnostics or monitoring.
The MOBILECT VIEWER is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Mobilect Viewer Ref K123082
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Nephosity, Inc. have in the registry?
The registry currently lists 1 device for Nephosity, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nephosity, Inc.'s devices?
Among its 1 most recently registered device, Nephosity, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Nephosity, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Nephosity, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Nephosity, Inc. in the registry?
The most recently registered devices listed for Nephosity, Inc. include MOBILECT VIEWER.