Tri-Staple 2.0 Reloads

Tri-Staple 2.0 Reloads is an FDA 510(k)-cleared medical device (K202864) 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 October 27, 2020. Regulation: 8.