Dunamis Force DFX Tensile Tape

Dunamis Force DFX Tensile Tape is an FDA 510(k)-cleared medical device (K153746) manufactured by Dunamis, 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 March 2, 2016. Regulation: 8.