
Covidien, Formerly Valleylab,
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LUGASURE CURVED, SMALL JAW, OPEN SEALER/DIVIDER is an FDA 510(k)-cleared medical device (K102470) manufactured by Covidien, Formerly Valleylab,. 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 February 6, 2011. Regulation: 8.