Cataract Surgery Device Enhancement Receives FDA Clearance

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Bausch and Lomb's Victus femtosecond laser platform has received clearance from the FDA for an enhanced patient interface kit.

Bausch and Lomb’s Victus femtosecond laser platform has received clearance from the FDA for an enhanced patient interface kit.

The Victus platform is indicated to create a corneal flap in patients undergoing cataract surgery. Its enhanced interface includes a small diameter suction clip, which allows it to open and close easier for better placement in patients with narrow fissures and smaller eye openings.

“The smaller profile in the enhanced patient interface…will allow surgeons to have even greater control and ease of use in patients with narrow fissures, further supporting improved suction and better overall comfort,” stated Jeffrey Whitman, president and chief surgeon at the Key-Whitman Eye Center in Dallas, Texas.

Additional features of the interface kit include a colored suction skirt, multi-port suction design, and ergonomical design, all of which assist surgeons throughout the eye procedure.

“We are very pleased to provide this advancement to our Victus femtosecond laser to surgeons and their patients,” stated Ari Kellen, head of US Eye Health at Bausch and Lomb. “…We are committed to investing in the technology and surgical enhancements to meet the needs of doctors and their patients.”

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