Clinical Research Directory

Key Inclusion Criteria: * Subjects must be 22 years of age or older * Able to comprehend and provide written informed consent * Willing and able to comply with schedule for follow-up visits * Demonstrate sufficient cognitive awareness to comply with examination procedures * Other inclusion criteria specified in the protocol may apply. Key Exclusion Criteria: * Subjects with clinically significant dry eye syndrome (DES) expected to impact postoperative visual acuity * Subjects taking medications that may affect ocular function (including but not limited to mydriatic, cycloplegic and miotic agents; tricyclic antidepressants, phenothiazines, benzodiazepines, first generation antihistamines, and anticholinergic agents) * Prior intraocular or corneal surgery (including corneal refractive correction i.e., LASIK, PRK, etc.) * Any corneal dystrophy that may affect visual acuity (e.g., keratoconus, pellucid corneal degeneration, etc.) * Other exclusion criteria specified in the protocol may apply.