Skip to content

Campillary Systems

Country not established

Devices
1

What Campillary Systems makes

Campillary Systems manufactures the Respirizor, a medical device designed for respiratory support or monitoring, likely intended for use in clinical or home settings to assist with breathing or ventilation.

The Respirizor is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. 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

  • Respirizor Ref K760095

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

Frequently asked questions

How many devices does Campillary Systems have in the registry?

The registry currently lists 1 device for Campillary Systems. Devices recorded under merged duplicate company entries are counted once.

Which registries list Campillary Systems's devices?

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

What risk classes do Campillary Systems's devices fall under?

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

What are the newest devices from Campillary Systems in the registry?

The most recently registered devices listed for Campillary Systems include RESPIRIZOR.

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