LigaSure™ XP Maryland Jaw Sealer/Divider

LigaSure™ XP Maryland Jaw Sealer/Divider is an FDA 510(k)-cleared medical device (K223158) manufactured by Covidien, LLC. 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 January 22, 2023. Regulation: 8.