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Hansen Medical's Magellan Robotic System Used for IVC Filter Retrieval

January 22, 2015—Hansen Medical announced the completion of the first intravascular robot-assisted retrieval of an inferior vena cava (IVC) filter using the company’s Magellan robotic system.

FDA Clears Corindus' CorPath GRX System in Peripheral Vascular Interventions

February 20, 2018—Corindus Vascular Robotics, Inc. announced that it has received 510(k) clearance from the US Food and Drug Administration for use of the company's CorPath GRX system in peripheral vascular interventions (PVIs).

Gore's DrySeal Sheath Cleared

May 11, 2010—W.

FDA Clears Gore's DrySeal Sheath

May 11, 2010—W.

Gore Launches DrySeal Sheath With Hydrophilic Coating

December 18, 2012—Gore & Associates (Flagstaff, AZ) introduced the Gore DrySeal sheath with hydrophilic coating, which is intended to allow easier insertion and removal during endovascular repair procedures.

Gore C3 Delivery System Approved in Japan

December 3, 2013—Gore & Associates (Flagstaff, AZ) announced that it has received Shonin regulatory approval from the Japanese Ministry of Health, Labor and Welfare to market the Gore Excluder abdominal aortic aneurysm (AAA) endoprosthesis featuring the Gore C3 delivery system as a minimally invasive treatment for AAA patients.

Gore Recognizes "Pioneers in Performance"

November 16, 2012—Gore & Associates (Flagstaff, AZ) announced the honorees of the 2011-2012 Pioneers in Performance Awards for the United States.

FDA Clears Hansen Medical's Magellan Robotic System for Peripheral Vascular Interventions

June 4, 2012—Hansen Medical, Inc. (Mountain View, CA) announced that it has received 510(k) clearance from the US Food and Drug Administration for its Magellan robotic system, including the catheter and accessories.