
Lensar, Inc.
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LENSAR LASER SYSTEM FOR ANTERIOR CAPSULOTOMY is an FDA 510(k)-cleared medical device (K102727) manufactured by Lensar, Inc.. This device is classified under the Ophthalmic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 15, 2011. Regulation: 8.