
Dornier Medtech America, Inc.
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DORNIER DIODE LASER FAMILY MEDILAS D, MEDILAS D SKINPULSE & MEDILAS D SKINPULSE S LASER SYSTEM is an FDA 510(k)-cleared medical device (K020339) 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 October 24, 2002. Regulation: 8.