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ClearPoint 2.0 Software Approved for Use In Europe

The ClearPoint 2.0 software, which received 510(k) clearance in 2018, recently obtained CE mark and is now available to our European customers. The software utilizes a hospital’s existing diagnostic-only or intraoperative MRI suite, and works to enable a range of minimally invasive procedures in the brain.

One of the main goals of the ClearPoint 2.0 project was to re-develop the software using a new visualization platform while improving functionality and ensuring compatibility with Windows 10. ClearPoint 2.0 optimizes existing workflows for more efficient clinical interaction with new feature sets including: image fusion, volume of interest (VOI) enhanced 3D viewing, multi-trajectory planning as well as an optimized user experience of the Navigation System.

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