On April 23, 2021, the FDA notified the company that its single step application wound irrigation solution, XPERIENCE No Rinse Antimicrobial Solution, has been 510(k) cleared in the U.S. for immediate distribution. The device was originally submitted to the FDA as MIS Solution but is now being marketed as XPERIENCE.
The company says the residual solution remains in the surgical site after closure and, “continues to help defend against pathogens for several hours, giving surgeons a simple and effective adjunct to help prevent surgical site and post-operative infections.” … read more