Xact Robotics, Ltd. is one of 267 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Xact Robotics, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: XACT Robotic System, ACE Model, XACT ACE Robotic System, XACT Robotic System
4
Total
4
Cleared
0
Denied
Xact Robotics, Ltd. has 4 FDA 510(k) cleared medical devices. Based in Caesarea, IL.
Last cleared in 2022. Active since 2019. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Xact Robotics, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Xact Robotics, Ltd.
4 devices