Study Status: Recruiting
Recruit Status: Recruiting
Study Type: Observational
Official Title: Device Exposure Registry: A Post-Approval Observational Registry of ReSure Sealant to Track the Incidence of Endophthalmitis After Sealing Corneal Incisions in Patients Un
Brief Summary: This is a prospective multicenter observational single arm post-approval registry that will collect post-approval data relative to the incidence of endophthalmitis for cataract surgery patients treated with the FDA-approved ReSure Sealant when used by a broad group of physicians under commercial use conditions.