Ultravena Industries, Ltd.
Country not established
- Devices
- 1
What Ultravena Industries, Ltd. makes
Ultravena Industries, Ltd. manufactures the OSTAR device, which is classified as a Class I medical device.
The OSTAR device is listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
Ostar Ref K955424
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ultravena Industries, Ltd. have in the registry?
The registry currently lists 1 device for Ultravena Industries, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ultravena Industries, Ltd.'s devices?
Among its 1 most recently registered device, Ultravena Industries, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Ultravena Industries, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Ultravena Industries, Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Ultravena Industries, Ltd. in the registry?
The most recently registered devices listed for Ultravena Industries, Ltd. include OSTAR.