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Cardio Source

Country not established

Devices
2

What Cardio Source makes

Cardio Source makes medical devices such as disposable valvulotomes and valvulotomes, which are used in cardiovascular procedures.

The company's portfolio is regulated as Class II devices and is listed in the FDA 510(k) registry, with the company based in the US.

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

Catalogue2

Newest first, rows 1-2 of 2

  • Annulus Disposable Valvulotome Ref K912635

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Annulus Valvulotome Ref K912636

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

Frequently asked questions

How many devices does Cardio Source have in the registry?

The registry currently lists 2 devices for Cardio Source. Devices recorded under merged duplicate company entries are counted once.

Which registries list Cardio Source's devices?

Among its 2 most recently registered devices, Cardio Source has devices listed in FDA 510(k) (2 devices).

What risk classes do Cardio Source's devices fall under?

Among its 2 most recently registered devices, the classes recorded for Cardio Source's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Cardio Source in the registry?

The most recently registered devices listed for Cardio Source include ANNULUS DISPOSABLE VALVULOTOME and ANNULUS VALVULOTOME.

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