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Cefla S.C.R.L.

Country not established

Devices
3

What Cefla S.C.R.L. makes

Cefla S.C.R.L. manufactures wound drainage systems (WDS) in sizes 2 and 2, as well as RX DC X-ray units designed for diagnostic imaging.

Their products are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. The company operates from the United States.

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

Catalogue3

Newest first, rows 1-3 of 3

  • C-U2 Ref K062897

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Wds, Size 2 And Size 2 Ref K061114

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Rx Dc X-Ray Unit Ref K080076

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

Frequently asked questions

How many devices does Cefla S.C.R.L. have in the registry?

The registry currently lists 3 devices for Cefla S.C.R.L.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Cefla S.C.R.L.'s devices?

Among its 3 most recently registered devices, Cefla S.C.R.L. has devices listed in FDA 510(k) (3 devices).

What risk classes do Cefla S.C.R.L.'s devices fall under?

Among its 3 most recently registered devices, the classes recorded for Cefla S.C.R.L.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Cefla S.C.R.L. in the registry?

The most recently registered devices listed for Cefla S.C.R.L. include C-U2, WDS, SIZE 2 AND SIZE 2 and RX DC X-RAY UNIT.

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