LENSAR Laser System Earns FDA 510(k) Clearance

The LENSAR Laser System, designed to help surgeons perform precise corneal and arcuate incisions during refractive cataract surgery, has earned FDA 510(k) clearance.

The LENSAR Laser System utilizes the company's Augmented Reality technology, which provides surgeons with biometric information and a high-resolution three-dimensional reconstruction of the eye's anatomy.

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