Innerscan, Inc.
Country not established
- Devices
- 1
What Innerscan, Inc. makes
Innerscan, Inc. makes Concept One, a medical device.
Concept One is a Class I device listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Concept One Ref K933777
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Innerscan, Inc. have in the registry?
The registry currently lists 1 device for Innerscan, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Innerscan, Inc.'s devices?
Among its 1 most recently registered device, Innerscan, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Innerscan, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Innerscan, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Innerscan, Inc. in the registry?
The most recently registered devices listed for Innerscan, Inc. include CONCEPT ONE.