Frequently Asked Questions
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What is the XACT ACE Robotic System’s approval?
FDA Cleared & CE Mark
The XACT ACE Robotic System has FDA clearance and CE Mark for use during CT-guided percutaneous procedures. It enables interventional radiology and interventional oncology teams to reach targets, regardless of size, depth, or location, with greater accuracy, consistency, and efficiency.
Where is the XACT ACE Robotic System available for purchase?
The XACT ACE Robotic System is available in the U.S. and EMEA.
Interested in learning more or scheduling a demo? Complete our request a demo form to have an XACT representative contact you.
What types of procedures has the XACT ACE Robotic System been leveraged for?
CT-guided percutaneous procedures
The XACT ACE® Robotic System can be leveraged for CT-guided percutaneous procedures, such as biopsy, ablation, and drainage procedures. The system has clinical experience in multiple organs throughout the lungs and abdomen. For examples of our clinical experience, view our case studies.
Are there specific instruments I need to purchase from XACT Robotics that are compatible with the system?
There is no need to validate or purchase new instruments.
The XACT ACE® Robotic System is instrument agnostic and designed to utilize instruments you already stock today. This helps to ensure physician preference remains intact and eliminates the need for additional investment.
What is ACE S Drive Enabled?
Patented technology exclusive to the XACT ACE® Robotic System
When a target shifts from its original location, our proprietary ACE S Drive™ technology enables the XACT ACE® Robot to quickly adapt from a linear to non-linear trajectory and steer the instruments accordingly to remain exactly on target.