Tecomet Global Unite Short Stem Instrumentation

Tecomet Global Unite Short Stem Instrumentation is an FDA 510(k)-cleared medical device (K211553) manufactured by Symmetry Medical Manufacturing Inc. Dba Tecomet, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 3, 2021. Regulation: 8.