User Acceptability Evaluation of Pseudophakic Patients Previously Implanted With the TECNIS Odyssey IOL

Exclusion Criteria

• •1. Concurrent participation in an interventional clinical trial during the time from which the data will be collected;
• •2. Use of systemic or ocular medication that may affect vision
• •3. Prior corneal refractive surgery in each eye (i.e., LASIK, PRK, SMILE, RK, CK); NOTE: Limbal relaxing incisions (LRI) are permissible as planned at the time of surgery (intraoperatively) but not postoperatively until after completion of the study visits;
• •4. Ongoing adverse events that might impact study measurements, as determined by the investigator;
• •5. Acute or chronic disease or condition, ocular trauma, or surgery that may confound study measurements (e.g., clinically significant macular degeneration, glaucoma, cystoid macular edema, proliferative diabetic retinopathy, keratoconus, etc.);
• •6. Amblyopia, strabismus, nystagmus in each eye