Lightfusion LED device given FDA clearance

Lightfusion has been cleared as a Class II medical device, suitable for the treatment of periorbital wrinkles, by the FDA.

The device is an advanced, non-invasive LED photo facial which harnesses light energy to alter biological activity in the skin to rejuvenate it. It delivers different wavelengths (633nm red light and 830nm near infra-red) of light to promote collagen and elastin synthesis; improve blood flow and eliminate toxins.

Lightfusion can be used as a standalone treatment, as part of a course, or as a compliment to enhance and accelerate other treatments. The Lightfusion device has been created with a modular design so it can be positioned on the face without being claustrophobic and can also be used to treat the neck, décolleté and hands. Lightfusion is used in combination with a unique vitage Hydrogel Mask, which delivers key ingredients to the skin including probiotics, plant extracts and marine collagen while allowing the maximum number of light protons through to the skin.

Amanda Coveney, managing director of Skinbrands, the UK distributor for Lightfusion, said the FDA endorsement was a “significant milestone”.