Spineart and eCential Robotics received FDA 510(k) clearance on August 26, 2026 for Spineart’s PERLA TL application to run on eCential’s Op.n navigation and robotic-assisted platform, extending a previously navigation-only pairing into robotic-assisted workflows. The clearance covers the PERLA TL Open and MIS pedicle screw systems in both open and minimally invasive spine procedures, the companies said in their joint announcement. The clearance changes what the PERLA app does on the Op.n…