
Dornier Surgical Products, Inc.
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DORNIER MEDILAS H/2 is an FDA 510(k)-cleared medical device (K984591) manufactured by Dornier Surgical Products, 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 March 25, 1999. Regulation: 8.