Machina Medical Receives FDA 510(k) Clearance for MFUSE External Bleeding Control Device

ROSWELL, Ga., Jan. 20, 2026 (GLOBE NEWSWIRE) -- Machina Medical, Corp. today announced it has received 510 (k) clearance from the U.S. Food and Drug Administration (FDA) for MFUSE, a sterile, ...
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Teleflex Receives FDA Clearance for Expanded Use of QuikClot Control+™ Hemostatic Device to Address All Grades of Bleeding

Teleflex Incorporated announced the FDA 510(k) clearance for an expansion of the QuikClot Control+™ Hemostatic Device's indications, now including all grades of internal and external bleeding.