Shots:

• The US FDA has granted 510(k) clearance to the company's IOPS Viewpoint Catheter, which reduces physician and patient exposure to harmful X-rays at the time of image-guided, endovascular procedures
• The catheter offers 3D navigation feedback for precision access and enables real-time visualization of endovascular tools when combined with IOPS software, reducing reliance on fluoroscopy and harmful radiation exposure during endovascular procedures
• The device improves visualization, minimizes procedure times, and decreases radiation exposure for patients & healthcare providers