Arjo receives 510(k) clearance from US FDA for WoundExpress
Arjo has received 510(k) clearance from the US Food and Drug Administration (FDA) for WoundExpress, an intermittent pneumatic compression (IPC) solution for accelerating healing of venous leg ulcers. The FDA clearance follows several recent studies showing that WoundExpress can significantly improve lower leg wound management. “This is an important milestone for us and we see great potential in now bringing this innovative therapy to the US market as well”, says Joacim Lindoff, President & CEO of Arjo. “Venous leg ulcers are a rapidly growing and costly problem for healthcare, with