A Real-World Evidence (RWE) Long-Term Follow-Up Study to Assess Outcomes of Alcon Monofocal Intraocular Lenses

Key Inclusion Criteria: * Subject is implanted with one of the study IOL models between 3 and 5 years previously. * Subject follow-up is expected to be possible during the duration of the study. * Subject or legally authorized representative must be able to understand and sign the IRB/EC approved Informed Consent form. Minor subjects will complete an Assent Form. * Documented medical history and required pre-operative baseline information is available for retrospective data collection. Key Exclusion Criteria: * Subject is participating in a separate investigational drug or device study. * Pregnancy at the time of enrollment.