A Multicenter, Observational, Single Arm Study of the TECNIS Presbyopia-correcting Intraocular Lens

Inclusion Criteria: * Patients who are bilaterally implanted with TECNIS PC IOL and are at least 45 days postoperative from their second eye surgery * Clear intraocular media * Signed informed consent and data protection documentation * Availability, willingness, ability, and sufficient cognitive awareness to comply with examination procedures * Ability to understand, read, and write English or the local language in which the informed consent and questionnaires are provided Exclusion Criteria: * Subjects with ongoing adverse events that might impact outcomes during the study * Use of systemic or ocular medication that may affect vision * Acute or chronic disease or condition, ocular trauma or surgery that may confound results * Patients with amblyopia, strabismus, nystagmus * Concurrent participation in another clinical trial