I.T.S. Group S.R.L.
ItalyFDA 510(k) applicant, unverified
- Devices
- 1
What I.T.S. Group S.R.L. makes
I.T.S. Group S.R.L. manufactures the Stardust Med device, a medical product designed for use in specific clinical applications.
The company’s portfolio is regulated under FDA 510(k) clearance as a Class II device and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Stardust Med Ref K200736
510(k) 510(k)
Frequently asked questions
How many devices does I.T.S. Group S.R.L. have in the registry?
The registry currently lists 1 device for I.T.S. Group S.R.L.. Devices recorded under merged duplicate company entries are counted once.
Which registries list I.T.S. Group S.R.L.'s devices?
Among its 1 most recently registered device, I.T.S. Group S.R.L. has devices listed in FDA 510(k) (1 device).
What risk classes do I.T.S. Group S.R.L.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for I.T.S. Group S.R.L.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from I.T.S. Group S.R.L. in the registry?
The most recently registered devices listed for I.T.S. Group S.R.L. include Stardust Med.