Biom'Up S.A. announced that the U.S. Food and Drug Administration (FDA) approved the IDE (Investigational Device Exemption) application for HEMOSNOW, a hemostatic dry powder made from porcine collagen and bovine-derived chondroitin sulfate developed by the Company for managing minimal and mild levels of bleeding during surgical procedures. The Company initially submitted the IDE application to FDA for HEMOSNOW in January 2019. HEMOSNOW will complement Biom'up's product, HEMOBLASTTM Bellows, as a hemostatic solution for use in minimal (oozing) to mild (pooling) bleeding. HEMOSNOW contains the same components as HEMOBLAST Bellows, but without human pooled plasma thrombin. It will thus be available at a lower cost and targeted at less severe bleedings. HEMOSNOW uses the exact same applicator system as HEMOBLAST Bellows, making it ready for use on focal bleeding sites as well as bleeding surfaces of up to 50 square centimeters per bellows.