www.fdanews.com/articles/185094-bausch-lomb-achieves-fda-clearance-for-crystalsert-injector
Bausch + Lomb Achieves FDA Clearance for Crystalsert Injector
January 4, 2018
The FDA issued 510(k) marketing clearance for the Bausch + Lomb Cystalsert 2.6 injector.
The first-of-its-kind FDA-cleared injector can be used across the company’s suite of intraocular lenses.
The CI-26 allows for easy wound entry and helps prevent tissue snagging via an incision as small as 2.6 mm, the company said.