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Biosaf IN S.r.l.

ItalyFDA applicant, unverified

Devices
1

What Biosaf IN S.r.l. makes

Biosaf IN S.R.L. manufactures the WINSIX Implant System, a medical device designed for surgical implantation.

The WINSIX Implant System is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the US.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • WINSIX Implant System Ref K133733

    Active Regimes: 510(k) Registry: 510(k) Class:II

Frequently asked questions

How many devices does Biosaf IN S.R.L. have in the registry?

The registry currently lists 1 device for Biosaf IN S.R.L.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Biosaf IN S.R.L.'s devices?

Among its 1 most recently registered device, Biosaf IN S.R.L. has devices listed in FDA 510(k) (1 device).

What risk classes do Biosaf IN S.R.L.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Biosaf IN S.R.L.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Biosaf IN S.R.L. in the registry?

The most recently registered devices listed for Biosaf IN S.R.L. include WINSIX Implant System.

Generated automatically from registry data and not verified by a human reviewer.