Unitron Corp.
Country not established
- Devices
- 1
What Unitron Corp. makes
Unitron Corp. makes the OMNI STIK device.
The OMNI STIK is a Class I medical device listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
Omni Stik Ref K781616
510(k) 510(k)
Frequently asked questions
How many devices does Unitron Corp. have in the registry?
The registry currently lists 1 device for Unitron Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Unitron Corp.'s devices?
Among its 1 most recently registered device, Unitron Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Unitron Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Unitron Corp.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Unitron Corp. in the registry?
The most recently registered devices listed for Unitron Corp. include OMNI STIK.