Coinciding with the FDA’s clearance for the catheter, Perfuze has also completed a €22m ($24m) financing round.

At the day of the survey, general data, catheter-related data, data on antibiotic use, and UTI data were collected for each patient using a standardized case record form. General variables ...

Perfuze announced today that it received FDA 510(k) clearance for its Zipline access catheter and secured significant funding ...

T-DOC ® Air-Charged™ disposable catheters use tiny pressure-sensing air balloons to assess internal pressures. Barely larger than the diameter of the catheter itself, these balloons offer ...

The team suggested poor hygiene and using a catheter long term could be to blame, as bacteria can easily enter the urinary tract and cause infections. Doctors believe there are only a handful of ...

Dr. SoHyun Boo, medical director for Neurointerventional Surgery in RNI's Department of Neuroradiology, explained the device and its use. The Broadway represents an advance on existing catheter ...

Johnson & Johnson MedTech‘s Shockwave Medical announced the U.S. launch of its Javelin peripheral intravascular lithotripsy ...

Olubadewa A. Fatunde and Win-Kuang Shen. Catheter Ablation as the First-Line Therapy for Atrial Fibrillation: Update on Evidence and Clinical Implications. CVIA. 2025. Vol. 10 (1). DOI: ...

In addition to the FDA 510(k) submission, Stereotaxis expects to submit the catheter for CE mark clearance in Europe this ...

Stereotaxis (NYSE: STXS), a pioneer and global leader in surgical robotics for minimally invasive endovascular intervention, ...

Stereotaxis (STXS) announced FDA regulatory submission for the first robotically navigated catheter designed to expand usage of Robotic ...