
FluidAI Medical’s Origin™ device has received FDA 510(k) clearance, a pivotal milestone redefining the future of data-driven, post-operative care
In the news release, Fluid AI Medical Receives FDA 510(k) Clearance for Origin™, a Real-Time Postoperative Bedside Monitoring Device, issued 24-Sep-2025 by Fluid AI Medical over PR Newswire, we are advised by the company that the news release has been updated.