Bausch + Lomb Receives FDA 510(k) Clearance for New Products
Bausch + Lomb Corporation announced that the U.S. Food and Drug Administration has granted 510(k) clearance for the Bi-Blade+ advanced dual-port vitrectomy cutter and the Adaptive Fluidics advanced update on the Stellaris Elite Vision Enhancement System. "Retinal surgeons who are familiar with our Bi-Blade technology understand the benefits of its dual-port design, 100% open duty cycle and cutting speed of 15,000 cuts per minute," said Wayne Caulder, vice president and general manager, North America Surgical, Bausch + Lomb.