Clinical Research Directory

Inclusion Criteria: * Male or female adults ages 45 years or older on the day of screening who have cataract(s) in one or both eyes or suffer from presbyopia; * Regular corneal astigmatism ≥0.75 dioptres (measured by an automatic keratometer or biometer) in one or both eyes; * Capability to understand and sign an IRB approved informed consent form and privacy authorization; * Clear intraocular media other than cataract; * Calculated IOL power is within the range of the study IOLs; * Dilated pupil size large enough to visualize IOL axis markings postoperatively; * Willing and able to conform to the study requirements. Exclusion Criteria: * Regular corneal astigmatism \<0.75 dioptres (measured by an automatic keratometer or biometer) in both eyes * Irregular astigmatism; * Subjects with diagnosed degenerative visual disorders (e.g. macular degeneration or other retinal or optic disorders) that are predicted to cause future acuity losses to a level of 20/30 or worse; * Subjects with AMD suspicious eyes as determined by OCT examination; * Subjects who may be expected to require retinal laser treatment during the course of the study or at a greater risk of developing cystoid macular edema; * Previous intraocular or corneal surgery; * Traumatic cataract; * History or presence of macular edema; * Pregnant, lactating or, if able to bear children, unwilling to use medically acceptable birth control over the course of the study; * Concurrent or previous (within 30 days) participation in another drug or device investigation; * Instability of keratometry or biometry measurements; * Ocular hypertension or glaucoma; * Significant dry eye; * Unsuitable for study participation for any other reason, as determined by Investigator's clinical judgment (reason to be documented on eCRF).