Skip to content

Omega Group, Inc.

Country not established

Devices
1

What Omega Group, Inc. makes

Omega Group, Inc. manufactures the ELITE COLLECTION, a line of Class I medical devices designed for specific clinical applications.

These devices are regulated under the FDA’s 510(k) pathway and are listed in the U.S. regulatory system. 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

  • Elite Collection Ref K936149

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

Frequently asked questions

How many devices does Omega Group, Inc. have in the registry?

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

Which registries list Omega Group, Inc.'s devices?

Among its 1 most recently registered device, Omega Group, Inc. has devices listed in FDA 510(k) (1 device).

What risk classes do Omega Group, Inc.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Omega Group, Inc.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Omega Group, Inc. in the registry?

The most recently registered devices listed for Omega Group, Inc. include ELITE COLLECTION.

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