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Breath of Life, Inc.

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Devices
1

What Breath of Life, Inc. makes

Breath of Life, Inc. manufactures the LIFEGUARD VENT MASK, a device designed for mechanical ventilation support in clinical settings. This product is intended for use with ventilators to deliver controlled breaths to patients requiring respiratory assistance.

The LIFEGUARD VENT MASK is classified as a Class II medical device under US regulations and has been authorised through the FDA’s 510(k) clearance process. The company is based in the United States.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Lifeguard Vent Mask Ref K883383

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

Frequently asked questions

How many devices does Breath of Life, Inc. have in the registry?

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

Which registries list Breath of Life, Inc.'s devices?

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

What risk classes do Breath of Life, Inc.'s devices fall under?

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

What are the newest devices from Breath of Life, Inc. in the registry?

The most recently registered devices listed for Breath of Life, Inc. include LIFEGUARD VENT MASK.

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