A Prospective Multicenter Study To Assess The Clinical Outcomes Of Current Phacoemulsification Approach To Cataract Extraction Versus The Micor System Device

The purpose of this research study is to evaluate the clinical outcomes of current phacoemulsification approaches to cataract extraction involving high-frequency thermogenic energy versus the use of the MICOR System device using low-energy segment removal with a micro-interventional irrigation/aspiration port to evacuate the lens in subjects undergoing routine cataract surgery.

Inclusion Criteria:Able to understand study requirements, willing to follow study instructions and willing to return for required study follow-up visits.Willing and able to understand and complete the informed consent document.Subjects with a cataract grade of 1 to 4+ and are scheduled to undergo cataract surgery.Subjects ≥ 18 years of age.Exclusion Criteria:Subjects, who in the opinion of the investigator, have "compromised" eye(s); no comorbidities and no patients undergoing concurrent corneal surgery with cataract extraction.Concurrent participation or participation in any clinical trial up to 30 days prior to preoperative visit.Subjects that are pregnant, lactating or planning to become pregnant during the course of the study.