
Covidien
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Valleylab FT10 Energy Platform, Valleylab FX8 FX Series Energy Platform is an FDA 510(k)-cleared medical device (K181389) manufactured by Covidien. 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 June 18, 2018. Regulation: 8.