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Medx Electronics, Inc.

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Devices
6

What Medx Electronics, Inc. makes

Medx Electronics, Inc. manufactures laser-based medical devices for dermatological and cosmetic procedures, including tethered and portable laser systems for skin treatments. Their product line includes consoles with laser accessories, standalone portable lasers, and specialized laser series for targeted applications like oral tissue procedures. Devices are designed for professional use in clinical and office-based settings, covering treatments such as hair removal, skin resurfacing, and vascular lesion management.

The company’s devices are classified as Class II under FDA regulations and are supported by 510(k) clearances. Products are listed in the FDA’s 510(k) database, indicating compliance with U.S. medical device authorization requirements. Medx Electronics, Inc. is headquartered in the United States.

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

Catalogue6

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Frequently asked questions

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

The registry currently lists 6 devices for Medx Electronics, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Medx Electronics, Inc.'s devices?

Among its 6 most recently registered devices, Medx Electronics, Inc. has devices listed in FDA 510(k) (6 devices).

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

Among its 6 most recently registered devices, the classes recorded for Medx Electronics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Medx Electronics, Inc. include MEDX HOME, MEDX LPT 200 TETHERED LASER & MEDX LPS 200 (ORALASE) PORTABLE LASER, MEDX1100 CONSOLE & MEDX 100T AND DUOLIGHT LASER ACCESSORIES, MEDX 100 PORTABLE LASER and NMA 1052 CONSOLE SYSTEM WITH NMA 100 LASER ACCESSORY.

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