Fusion Robotics, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Fusion Robotics, LLC - FDA 510(k) Cleared Devices
Recent clearances: Remi Robotic Navigation System, Remi Robotic Navigation System
2
Total
2
Cleared
0
Denied
Fusion Robotics, LLC has 2 FDA 510(k) cleared medical devices. Based in Louisville, US.
Last cleared in 2023. Active since 2022. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Fusion Robotics, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Integrity Implants Inc. Dba Accelus as regulatory consultant.
FDA 510(k) Regulatory Record - Fusion Robotics, LLC
2 devices