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 dayspostoperative from their second eye surgery

• Clear intraocular media

• Signed informed consent and data protection documentation

• Availability, willingness, ability, and sufficient cognitive awareness to complywith examination procedures

• Ability to understand, read, and write English or the local language in which theinformed 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 confoundresults

• Patients with amblyopia, strabismus, nystagmus

• Concurrent participation in another clinical trial