Bausch + Lomb Boston Scleral Lens Case

Bausch + Lomb Boston Scleral Lens Case is an FDA 510(k)-cleared medical device (K173365) manufactured by Bausch & Lomb, Incorporated. This device is classified under the Ophthalmic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 16, 2017. Regulation: 8.