The Only Adjustable Lens for Cataract Surgery🔒 SSL Verified

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"RxSight develops the Light Adjustable Lens™ (LAL®)—the only FDA-approved intraocular lens (IOL) that can be customized after cataract surgery.Unlike fixed lenses, the LAL allows your surgeon to fine-tune your prescription after your eye has healed, based on real outcomes rather than pre-surgical estimates."

"INDICATIONS: The Light Adjustable Lens™ (LAL®) and Light Delivery Device™ (LDD™) system is indicated for the reduction of residual astigmatism to improve uncorrected visual acuity after removal of the cataractous natural lens by phacoemulsification and primary implantation of the intraocular lens in the capsular bag in adult patients with preexisting corneal astigmatism of ≥ 0.75 diopters and without preexisting macular disease. The system also reduces the likelihood of clinically significant residual spherical refractive errors."

"CONTRAINDICATIONS: The LAL is contraindicated in patients who are taking systemic medication that may increase sensitivity to ultraviolet (UV) light as the LDD treatment may lead to irreversible phototoxic damage to the eye; patients who are taking a systemic medication that is considered toxic to the retina (e.g., tamoxifen) as they may be at increased risk of retinal damage during LDD treatment; patients with a history of ocular herpes simplex virus due to the potential for reactivation from exposure to UV light; patients with nystagmus as they may not be able to maintain steady fixation during LDD treatment; and patients who are unwilling to comply with the postoperative regimen for adjustment and lock-in treatments and wearing of UV protective eyewear."

"WARNINGS: Careful preoperative evaluation and sound clinical judgment should be used by the surgeon to decide the risk/benefit ratio before implanting an IOL in a patient with any of the conditions described in the LAL and LDD Professional Use Information document. Caution should be used in patients with eyes unable to dilate to a pupil diameter of ≥ 7 mm to ensure that the edge of the LAL can be visualized during LDD light treatments; patients who the doctor believes will be unable to maintain steady fixation that is necessary for centration of the LDD light treatment; and patients with sufficiently dense cataracts that preclude examination of the macula as patients with preexisting macular disease may be at increased risk for macular disease progression. Patients at high risk for future vitreoretinal disease that may require silicone oil as part of therapy. The LAL must be implanted in the correct orientation with the back layer facing posteriorly. There is no clinical data to demonstrate the safety and effectiveness of ciliary sulcus placement of the LAL. Patients with any of the following conditions may not be suitable candidates for the LAL: recurrent severe anterior or posterior segment inflammation or uveitis of unknown origin, or any disease producing an inflammatory reaction in the eye; surgical difficulties at the time of cataract surgery before LAL implantation; a compromised eye; eyes with neither the posterior capsule nor the zonules are intact enough to provide support for the LAL."

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