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