Silvestrin Fabris S.R.L.
Last updated 22 Oct 2026
- Devices
- 1
- Registries
- FDA 510(k)
- FDA recalls
- 0
Catalogue
Silfab Super 2 Max Compressor, N28 Series Ref K050183
What Silvestrin Fabris S.R.L. makes
Silvestrin Fabris S.R.L. manufactures the SILFAB SUPER 2 MAX COMPRESSOR, part of the N28 series, which is designed for medical gas compression applications.
The company’s portfolio is regulated under FDA 510(k) clearance as a Class II medical device. The devices are listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Frequently asked questions
How many devices does Silvestrin Fabris S.R.L. have in the registry?
The registry currently lists 1 device for Silvestrin Fabris S.R.L.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Silvestrin Fabris S.R.L.'s devices?
Among its 1 most recently registered device, Silvestrin Fabris S.R.L. has devices listed in FDA 510(k) (1 device).
What risk classes do Silvestrin Fabris S.R.L.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Silvestrin Fabris S.R.L.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Silvestrin Fabris S.R.L. in the registry?
The most recently registered devices listed for Silvestrin Fabris S.R.L. include SILFAB SUPER 2 MAX COMPRESSOR, N28 SERIES.