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Media Lab S.r.l.

ItalyFDA applicant, unverified

Devices
1

What Media Lab S.r.l. makes

Media Lab S.R.L. manufactures 3D-printed implantable devices, designed for surgical applications requiring custom or complex geometries.

These products are classified as Class II under FDA regulations and are authorised via 510(k) clearance. The company is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Implant 3D Ref K153091

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

Frequently asked questions

How many devices does Media Lab S.R.L. have in the registry?

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

Which registries list Media Lab S.R.L.'s devices?

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

What risk classes do Media Lab S.R.L.'s devices fall under?

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

What are the newest devices from Media Lab S.R.L. in the registry?

The most recently registered devices listed for Media Lab S.R.L. include IMPLANT 3D.

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