The Power to Stop Bleeding Throughout the World

A key part of Z-Medica's near-term growth strategy is developing markets on a worldwide scale. We are committed to making Z-Medica a global leader in hemorrhage control. Building our sales and support structures to meet the diverse needs of markets on every continent will make our products the preferred hemostatic devices worldwide.

QuikClot: Delivery of an Effective Hemostatic Agent
As the recommended hemostatic dressing for the U.S. Military, more than six million units of QuikClot Combat Gauze have been deployed since 2008. QuikClot is also used throughout the world in hospitals, law enforcement, disaster recovery and first responder kits, making QuikClot a key component of hemorrhage control solutions everywhere.

QuikClot devices use a proprietary methodology to impregnate gauze with kaolin, an inorganic mineral that accelerates the body’s natural clotting ability1,2 and produces no exothermic reaction. Since QuikClot does not contain animal proteins, human proteins, shellfish or botanicals, hemostasis can be achieved without worry of instigating an allergic response.1,2

  1. Trabattoni D, Montorsi P, Fabbiocchi F, Lualdi A, Gatto P, Bartorelli A. A new kaolin-based haemostatic bandage compared with manual compression for bleeding control after percutaneous coronary procedures. Eur Radiol. 2011;21:1687-1691.
  2. Lamb KM, Pitcher HT, Cavarocchi NC, Hirose H. Vascular site hemostasis in percutaneous extracorporeal membrane oxygenation therapy. Open Cardiovasc Thorac Surg J. 2012;5:8-10.


Z-Medica President & CEO Stephen J. Fanning Named As Semifinalist for Regional Ernst & Young Entrepreneur of the Year®

Z-Medica, LLC, a leading developer and marketer of hemostatic devices, announces that the Company’s President and CEO Stephen J. Fanning has been named as a semifinalist for the New York region Ernst & Young Entrepreneur of the Year® 2017.



Z-Medica Products Approved For Use In Brazil

Z-Medica announces today that a portfolio of QuikClot® products has been approved by the National Health Surveillance Agency (ANVISA), the Brazilian regulatory agency responsible for medical devices.



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