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Leoni Cia Cable System

FranceFDA applicant, unverified

Devices
1

What Leoni Cia Cable System makes

Leoni Cia Cable System manufactures the LEONI ORION System, a medical-grade cable assembly designed for use in surgical and interventional procedures, including minimally invasive applications.

The LEONI ORION System is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. 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

  • LEONI ORION System Ref K160518 Open recall

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

Frequently asked questions

How many devices does Leoni Cia Cable System have in the registry?

The registry currently lists 1 device for Leoni Cia Cable System. Devices recorded under merged duplicate company entries are counted once.

Which registries list Leoni Cia Cable System's devices?

Among its 1 most recently registered device, Leoni Cia Cable System has devices listed in FDA 510(k) (1 device).

What risk classes do Leoni Cia Cable System's devices fall under?

Among its 1 most recently registered device, the classes recorded for Leoni Cia Cable System's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Leoni Cia Cable System in the registry?

The most recently registered devices listed for Leoni Cia Cable System include LEONI ORION System.

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