Bausch + Lomb PreVue Inserter for enVista Preloaded

Bausch + Lomb PreVue Inserter for enVista Preloaded is an FDA 510(k)-cleared medical device (K192005) manufactured by Bausch & Lomb, Inc.. This device is classified under the Ophthalmic specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on October 3, 2019. Regulation: 8.