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Solta Medical Fraxel re:store Dual laser system receives FDA 510(k) clearance

Solta Medical, a provider of fractional resurfacing and non-invasive skin tightening and a provider in aesthetic skin treatments, has received FDA 510(k) clearance of its Fraxel re:store Dual laser system for the treatment of actinic keratosis (AKs).

The Fraxel system takes the fractional laser technology to the next level by adding a 1927nm wavelength, the first ever application of a Thulium laser in the aesthetics market.

Solta Medical claims that the Fraxel re:store Dual treatment provides superior results for the removal of Aks.

Solta Medical board chairman, president and CEO Stephen Fanning said that Solta Medical continues to develop safe, anti-aging solutions that deliver the best possible results in non-invasive aesthetic treatments.

“With the FDA clearance of our Fraxel re:store Dual system, we are providing our physicians with technology that patients are seeking, specifically in terms of reversing sun damage and treating precancerous skin lesions,” Fanning said.