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Equilasers, Inc.

Country not established

Devices
1

What Equilasers, Inc. makes

Equilasers, Inc. manufactures the Equilaser System, a medical device designed for laser-based procedures, likely targeting specific soft tissue applications such as dermatological or cosmetic treatments.

The Equilaser System is classified as a Class II 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.

Catalogue1

Newest first, rows 1-1 of 1

  • Equilase System Ref K022464

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

Frequently asked questions

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

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

Which registries list Equilasers, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Equilasers, Inc. include EQUILASE SYSTEM.

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