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Bresagen, Inc.

Country not established

Devices
1

What Bresagen, Inc. makes

Bresagen, Inc. manufactures the BRESAGEN CATHETER, Model CS-3000, a medical device designed for specific interventional procedures.

The device falls under FDA Class II regulation and is listed via the 510(k) pathway. The company is based in the United States.

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

Catalogue1

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Frequently asked questions

How many devices does Bresagen, Inc. have in the registry?

The registry currently lists 1 device for Bresagen, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Bresagen, Inc.'s devices?

Among its 1 most recently registered device, Bresagen, Inc. has devices listed in FDA 510(k) (1 device).

What risk classes do Bresagen, Inc.'s devices fall under?

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

What are the newest devices from Bresagen, Inc. in the registry?

The most recently registered devices listed for Bresagen, Inc. include BRESAGEN CATHETER, MODEL CS-3000.

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