Early Feasibility Study of UV-Femtosecond Laser Assisted Lenticular Extraction

Exclusion Criteria

• •Pregnant or nursing;
• •Acute or chronic disease or illness that would increase the operative risk or confound the outcomes of the study as clinically assessed by the Investigator;
• •Active implanted device, including but not limited to, heart pacemaker or defibrillator, for which laser use may be a contraindication;
• •Current use of medications with known ocular side effects;
• •Predicted residual stromal bed thickness \<300 micrometers (μm) in study eye
• •Ocular conditions in the study eye;
• •Previous ocular surgery in the study eye that resulted in corneal distortions within the treatment zone;
• •Residual, recurrent or active ocular disease that may impact study outcomes;
• •Previous or current diagnosis of dry eye;
• •Known allergic reaction to medications expected to be used preoperatively, during laser refractive surgery, and for postoperative care;
• •Pre-existing corneal opacities in study eye;
• •Contact lens worn in study eye and not removed prior to study testing affected by wear per timeframe specified in the protocol;