Skip to content

Edwards Ventilator Co.

Country not established

Devices
1

What Edwards Ventilator Co. makes

Edwards Ventilator Co. manufactures the Lakeville Body Ventilator, a mechanical ventilator designed for respiratory support in clinical settings.

The Lakeville Body Ventilator is classified as a Class II medical device and is listed under 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

  • Lakeville Body Ventilator Ref K840885

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

Frequently asked questions

How many devices does Edwards Ventilator Co. have in the registry?

The registry currently lists 1 device for Edwards Ventilator Co.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Edwards Ventilator Co.'s devices?

Among its 1 most recently registered device, Edwards Ventilator Co. has devices listed in FDA 510(k) (1 device).

What risk classes do Edwards Ventilator Co.'s devices fall under?

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

What are the newest devices from Edwards Ventilator Co. in the registry?

The most recently registered devices listed for Edwards Ventilator Co. include LAKEVILLE BODY VENTILATOR.

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