“This newest generation of advanced technology IOLs now allows ophthalmic surgeons to simultaneously address multiple issues.”
- Warren E. Hill, MD

RESOURCES

	AcrySof® IQ Toric Brochure Get the facts on AcrySof® IQ Toric, including specs and studies.
	AcrySof® IQ Toric A-Constant FAQ Calculate a personalized A-Constant for AcrySof® IQ Toric.
	AcrySof® IQ Toric Patient Education Brochure Provide your patients with more information on cataract surgery and premium IOLs.
	AcrySof® IQ Toric Calculator Makes precise surgical planning easy.

Where the Best Micro-Surgical Components Come Together as One

As part of the INTREPID^® Micro-Coaxial System, AcrySof^® IOLs offer advanced optics on a proven platform, to provide excellent ease of implantation and proven patient benefits.

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Copyright © 2009 Alcon, Inc., a global company based in Hünenberg, Switzerland. Information contained here pertains to Alcon’s global operations and Alcon’s global product line. Not all products are approved in every market and approved labeling and instructions may vary by local country.

Currently AcrySof^® IQ Toric IOL is only available in the United States.

CAUTION: Federal law restricts this device to sale by or on the order of a physician. INDICATIONS: AcrySof^® IQ Toric IOL Models SN6AT3, SN6AT4, and SN6AT5 Posterior Chamber Intraocular lenses are intended for primary implantation in the capsular bag of the eye for the visual correction of aphakia and pre-existing corneal astigmatism secondary to the removal of a cataractous lens in adult patients with or without presbyopia, who desire improved uncorrected distance vision, reduction of residual refractive cylinder and increased spectacle independence for distance vision. WARNINGS: Careful preoperative evaluation and sound clinical judgment should be used by the surgeon to decide the risk/benefit ratio before implanting a lens in a patient with any of the conditions described in the Directions for Use labeling. Toric IOLs should not be implanted if the posterior capsule is ruptured, if the zonules are damaged, or if a primary posterior capsulotomy is planned. Rotation can reduce astigmatic correction; if necessary lens repositioning should occur as early as possible prior to lens encapsulation. All viscoelastics should be removed from both the anterior and posterior sides of the lens; residual viscoelastics may allow the lens to rotate. PRECAUTIONS: Studies have shown that color vision discrimination is not adversely affected in individuals with the AcrySof^® Natural IOL and normal color vision. The effect on vision of the AcrySof^® Natural IOL in subjects with hereditary color vision defects and acquired color vision defects secondary to ocular disease (e.g., glaucoma, diabetic retinopathy, chronic uveitis, and other retinal or optic nerve diseases) has not been studied. Do not resterilize; do not store over 45° C; use only sterile irrigating solutions such as BSS^® or BSS PLUS^® Sterile Intraocular Irrigating Solutions. ATTENTION: Reference the Directions for Use labeling for a complete listing of indications, warnings and precautions.