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Microvaper Devices

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Devices
1

What Microvaper Devices makes

Microvaper Devices manufactures portable nebulizers, including the POCKET NEB, designed for on-the-go respiratory therapy delivery.

The company’s products are regulated as Class II medical devices in the US and are listed under FDA 510(k) clearance. The manufacturer 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

  • Pocket Neb Ref K142541

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

Frequently asked questions

How many devices does Microvaper Devices have in the registry?

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

Which registries list Microvaper Devices's devices?

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

What risk classes do Microvaper Devices's devices fall under?

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

What are the newest devices from Microvaper Devices in the registry?

The most recently registered devices listed for Microvaper Devices include POCKET NEB.

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