www.fdanews.com/articles/187698-candela-cleared-for-pulsed-dye-laser
Candela Cleared for Pulsed Dye Laser
July 20, 2018
Candela received FDA’s 510(k) clearance for its Vbeam Prima device, a pulsed dye laser used to treat a range of skin conditions.
The 595 nm pulsed dye laser device is cleared for treating conditions like rosacea, acne, spider veins, port-wine stains, wrinkles, warts and stretch marks, as well as photo aging and benign pigmented lesions.
The Vbeam Prima adds a 1064 nm wavelength and advanced features not included in the Vbeam, including contact and spray cooling and once-a-day calibration.