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.

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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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