- In August 2024, Resivant Medical received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its first products: the Cutiva Topical Skin Adhesive and the Cutiva PLUS Skin Closure System. The latter uniquely combines an adhesive mesh patch with the high-viscosity Cutiva liquid adhesive.
- In March 2024, TELA Bio, Inc. introduced its LIQUIFIX FIX8 Laparoscopic and LIQUIFIX Precision Open Hernia Mesh Fixation Devices in the United States. Remarkably, LIQUIFIX is the first adhesive-based product approved for securing mesh without penetrating patient tissue, providing a strong and secure application.
