A Clinical Outcome Study of Two Multifocal Intraocular Lenses (IOL) in Cataract Patients

Inclusion Criteria: * Willing and able to understand and sign informed consent, and attend postoperative examinations per protocol schedule; * Requires cataract extraction followed by posterior intraocular lens implantation used as an on-label procedure in both eyes; * Willing to have second eye surgery within 45 days of first eye surgery; * Expected postoperative astigmatism \< 1.0 D in both eyes, as measured by keratometry; * Free of severe diseases(s)/condition(s) listed in the Warnings and Precautions section of the package inserts; * Other protocol-defined inclusion criteria may apply. Exclusion Criteria: * Refractive lens exchange (monocular DCVA of worse than 20/20, or ≥ 0.06 logMAR). This exclusion did not apply to binocular (OU) measurement; * Significant irregular corneal astigmatism as demonstrated by corneal topography; * Severe degenerative visual disorders; * Previous corneal surgery; * Amblyopia; * Planned multiple procedures, including LRI, LASIK, etc, during surgery or the course of the study; * History of corneal disease; * Severe diabetic retinopathy; * History of retinal detachment; * Severe conditions or acute or chronic diseases or illnesses that, per investigator's clinical judgment, would increase the operative risk or confound the results of the study; * Pregnant or planning pregnancy during course of study; * Other protocol-defined exclusion criteria may apply.