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Vomaris Innovations, Inc.

United StatesFDA 510(k) applicant, unverified

Devices
2

What Vomaris Innovations, Inc. makes

Vomaris Innovations, Inc. manufactures the Procellera, a device designed for cardiac electrophysiology procedures, including catheter ablation and mapping of the heart’s electrical activity.

The Procellera is classified as a Class II (U) 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.

Catalogue2

Newest first, rows 1-2 of 2

  • Procellera Ref K160783

    Unclassified
    Active 510(k) 510(k) —

  • Procellera Ref K130350

    Unclassified
    Active 510(k) 510(k) —

Frequently asked questions

How many devices does Vomaris Innovations, Inc. have in the registry?

The registry currently lists 2 devices for Vomaris Innovations, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Vomaris Innovations, Inc.'s devices?

Among its 2 most recently registered devices, Vomaris Innovations, Inc. has devices listed in FDA 510(k) (2 devices).

What are the newest devices from Vomaris Innovations, Inc. in the registry?

The most recently registered devices listed for Vomaris Innovations, Inc. include Procellera.

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