DORNIER MEDILAS D LITEBEAM+ 1470

DORNIER MEDILAS D LITEBEAM+ 1470 is an FDA 510(k)-cleared medical device (K110364) manufactured by Dornier Medtech America, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 6, 2011. Regulation: 8.