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Umeco, Inc.

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Devices
1

What Umeco, Inc. makes

Umeco, Inc. manufactures the UMECO OPTIMA 694 RUBY LASER SYSTEM, a medical laser device designed for surgical and dermatological procedures.

The company’s portfolio is regulated under FDA’s Class II device classification, with the UMECO OPTIMA 694 RUBY LASER SYSTEM listed via a 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

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Frequently asked questions

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

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

Which registries list Umeco, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Umeco, Inc. include UMECO OPTIMA 694 RUBY LASER SYSTEM.

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