DEKA Medical aesthetic laser family receives additional FDA approval

April 21, 2015

Aesthetic laser systems maker DEKA Medical has received an additional FDA clearance for its Synchro REPLA:Y laser systems.

BioOptics World Editors

Aesthetic laser systems maker DEKA Medical (Carlsbad, CA) has received an additional FDA clearance for its Synchro REPLA:Y laser systems, allowing for unprecedented maximum power of 180 W and a 24 mm spot size.

The Synchro REPLA:Y offering includes:

The Excellium 3.4, which includes a 3 Hz, 125 W, 755 mm alexandrite laser; a 180 W, 1064 nm Nd:YAG laser; and a FT pulsed light with five interchangeable filters;
The Excellium HP, a 180 W, 1064 nm Nd:YAG laser, with FT pulsed light capabilities; and
The Premium 1.4.2., equipped with a 3 Hz, 125 W, 755 mm alexandrite laser and FT pulsed light capabilities.

Each workstation offers high-speed, stable long-term, or permanent hair reduction, and treatment of pseudofolliculitis barbae (PFB). They also offer safe treatment of benign pigmented lesions, wrinkles, and photocoagulation of dermatological vascular lesions.

For more information, please visit http://dekamedinc.com.

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BioOptics World Editors

We edited the content of this article, which was contributed by outside sources, to fit our style and substance requirements. (Editor’s Note: BioOptics World has folded as a brand and is now part of Laser Focus World, effective in 2022.)