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Dominion Aesthetic Technologies, Inc.

United StatesFDA 510(k) applicant, unverified

Devices
3

What Dominion Aesthetic Technologies, Inc. makes

Dominion Aesthetic Technologies, Inc. manufactures radiofrequency-based aesthetic devices, including the Eon FR and EON systems, designed for non-surgical skin tightening and volume enhancement procedures.

These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue3

Newest first, rows 1-3 of 3

  • Eon FR Ref K180511

    Class II
    Active 510(k) 510(k) II
  • Eon Ref K211681

    Class II
    Active 510(k) 510(k) II
  • Eon Ref K222226

    Class II
    Active 510(k) 510(k) II

Frequently asked questions

How many devices does Dominion Aesthetic Technologies, Inc. have in the registry?

The registry currently lists 3 devices for Dominion Aesthetic Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Dominion Aesthetic Technologies, Inc.'s devices?

Among its 3 most recently registered devices, Dominion Aesthetic Technologies, Inc. has devices listed in FDA 510(k) (3 devices).

What risk classes do Dominion Aesthetic Technologies, Inc.'s devices fall under?

Among its 3 most recently registered devices, the classes recorded for Dominion Aesthetic Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Dominion Aesthetic Technologies, Inc. in the registry?

The most recently registered devices listed for Dominion Aesthetic Technologies, Inc. include Eon FR and EON.

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