RxSight, Inc.

RxSight, Inc. announced that the U.S. Food and Drug Administration (FDA) has approved the RxSight™ Light Adjustable Lens and the Light Delivery Device (LDD) for patients with pre-existing astigmatism of ≥ 0.75 diopters undergoing cataract surgery. This action ushers in a new era in the treatment of cataracts, as RxSight's Light Adjustable Lens is the first and only FDA approved intraocular lens (IOL) that can be adjusted post-operatively to improve uncorrected visual acuity

Read More: RxSight, Inc. Press Release; as mentioned in FDA News Release