• Teleflex's QuikClot Control+ Hemostatic Device received FDA 510(k) clearance for expanded use in all grades of internal and external bleeding, significantly broadening its clinical applications beyond severe bleeding scenarios.
• The expanded indication was supported by real-world evidence from a rigorous observational study of 603 emergency, trauma, and surgical patients across multiple U.S. sites, demonstrating safety and efficacy.
• This regulatory milestone is expected to add more than $150 million to Teleflex's serviceable addressable market in the United States, extending the device's use to general, gynecologic, and orthopedic surgeries.