AVL200 IOL for Treatment of Cataract and Presbyopia

This study is to evaluate the performance of the AVL200 IOL in terms of visual function improvement over a range of focal points. Participants meeting eligibility criteria will undergo cataract surgery with implantation of the AVL200 intraocular lens (IOL), then be followed through 1 year postoperatively. Postoperative assessments include safety and visual function.

Inclusion Criteria:Visually significant cataractBest corrected distance visual acuity between 20/40 and 20/200Potential distance visual acuity of 20/32 or betterCorneal astigmatism ≤ 1.5 dioptersExclusion Criteria:Use of medication that could affect accommodationPrevious corneal surgery or significant corneal abnormalitiesOcular pathology or degenerative disorder having potential to impair visual acuityPupil abnormalityIntraoperative cataract surgery complications that could affect IOL implantation or positioning