
Covidien
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Signia Small Diameter Reloads Including Regular (Round) Tip Version is an FDA 510(k)-cleared medical device (K222641) 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 November 28, 2022. Regulation: 8.