VisuMax Femtosecond Laser

VisuMax Femtosecond Laser is an FDA 510(k)-cleared medical device (K173371) manufactured by Carl Zeiss Meditec, Inc.. This device is classified under the Ophthalmic specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on April 12, 2018. Regulation: 8.