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Onocor Vascular, LLC

Country not established

Devices
1

What Onocor Vascular, LLC makes

Onocor Vascular, LLC manufactures the ONO Retrieval Device, a mechanical retrieval system designed for removing intravascular thrombi or emboli in vascular procedures.

The company’s portfolio is regulated under FDA Class II devices, with the ONO Retrieval Device authorised via the 510(k) pathway. The manufacturer 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

  • ONO Retrieval Device Ref K212988

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

Frequently asked questions

How many devices does Onocor Vascular, LLC have in the registry?

The registry currently lists 1 device for Onocor Vascular, LLC. Devices recorded under merged duplicate company entries are counted once.

Which registries list Onocor Vascular, LLC's devices?

Among its 1 most recently registered device, Onocor Vascular, LLC has devices listed in FDA 510(k) (1 device).

What risk classes do Onocor Vascular, LLC's devices fall under?

Among its 1 most recently registered device, the classes recorded for Onocor Vascular, LLC's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Onocor Vascular, LLC in the registry?

The most recently registered devices listed for Onocor Vascular, LLC include ONO Retrieval Device.

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