Unisen, Inc.
Country not established
- Devices
- 1
What Unisen, Inc. makes
Unisen, Inc. manufactures the STARTRAC, a medical device designed for patient monitoring or diagnostic purposes, though specific clinical applications are not detailed.
The STARTRAC device is classified under FDA Class I and is listed via a 510(k) pathway in the United States. The company is based in the US.
Catalogue
Startrac Ref K890793
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Unisen, Inc. have in the registry?
The registry currently lists 1 device for Unisen, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Unisen, Inc.'s devices?
Among its 1 most recently registered device, Unisen, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Unisen, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Unisen, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Unisen, Inc. in the registry?
The most recently registered devices listed for Unisen, Inc. include STARTRAC.