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The company developed the ReVene Thrombectomy Catheter for single-session mechanical removal of venous clots. Clinical feasibility data from a trial with a 12-month follow-up on nineteen patients showed all primary endpoints were met with no safety issues. The device received FDA clearance in December 2020 and CE Mark in May 2021. It was designed to minimize or eliminate the need for thrombolytic drugs and ICU care by efficiently removing large-volume clots without capital equipment.
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