Nsite, Inc.
Country not established
- Devices
- 1
What Nsite, Inc. makes
Nsite, Inc. produces the NSite Scoliosis Assessment App, a mobile software application designed for assessing scoliosis.
The company's device is classified as a Class U medical device and is listed in the FDA 510(k) registry. Nsite, Inc. is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
NSite Scoliosis Assessment App Ref K230463
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Nsite, Inc. have in the registry?
The registry currently lists 1 device for Nsite, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nsite, Inc.'s devices?
Among its 1 most recently registered device, Nsite, Inc. has devices listed in FDA 510(k) (1 device).
What are the newest devices from Nsite, Inc. in the registry?
The most recently registered devices listed for Nsite, Inc. include NSite Scoliosis Assessment App.