GMReis Receives FDA 510(k) Clearance for the VersaLock® Sterile Plating System, Advancing Its Single-Use Trauma Strategy for U.S. ASCs

GMReis has received FDA 510(k) clearance K262537 for the VersaLock® Sterile Plating System, completing 510(k)-cleared sterile implant solutions across its upper and lower extremity plating portfolio and laying the groundwork for procedure-specific single-use trauma sets built for Ambulatory Surgery Centers.