The purpose of this study is to evaluate the visual quality and function of pseudophakic patients.

Inclusion Criteria:

• Minimum 22 years of age
• Pseudophakic patients who have been bilaterally implanted with the same type of intraocular lenses in both eyes
• Ability to understand, read and write English to give consent and complete the study questionnaires
• Availability, willingness, and sufficient cognitive awareness to comply with examination procedures and study visits
• Signed informed consent and Health Insurance Portability and Accountability Act (HIPAA) authorization
• Other protocol-defined inclusion criteria might apply

Exclusion Criteria:

• Any ocular pathology of clinical significance, as determined by the investigator, that may affect visual outcomes or influence subjective ocular/visual symptoms
• Patient is pregnant or is lactating
• Concurrent participation or participation within 30 days prior in any other clinical trial
• Other protocol-defined exclusion criteria might apply

Bilaterally-implanted pseudophakic subjects over 22 years of age who meet the inclusion criteria.