Intuitive receives CE mark for transvaginal use of da Vinci SP system
September 20, 2026
The approval allows the da Vinci SP system to be utilised in more women’s health procedures across Europe.
The approval allows the da Vinci SP system to be utilised in more women’s health procedures across Europe.
Medtronic (NYSE: MDT) has received an FDA green light to bring its vessel-sealing technology over to its Hugo surgical robot, adding to the platform’s U.S. catalog of energy instruments.
Neptune Medical has landed an FDA clearance for its robotic system designed to provide stable control during colonoscopy.
XCath Robotics has FDA Breakthrough Device Designation for its in-development Iris surgical robotic system for mechanical thrombectomy to treat acute ischemic stroke.
With the FDA designate in hand, XCath will further the development of its system that is intended to broaden access to stroke treatment globally.
Danish medtech company Ropca will bring its autonomous musculoskeletal ultrasound system to the U.S. after receiving FDA 510(k) clearance
GENEVA, Aug. 26, 2026 /PRNewswire/ — Spineart, a global fast-growing company in spine surgery innovation, and eCential Robotics today announced that the U.S. Food and Drug Administration (FDA) has granted 510(k) clearance for the PERLA® TL application (PERLA® by Spineart app) for use with the eCential® Op.n® Navigation and Robotic-Assisted Platform.
The FDA granted de novo classification to a standalone robotic device that can draw blood from a patient’s arm without a hands-on operator.
Johnson & Johnson MedTech (NYSE: JNJ) today announced the launch of Monarch Quest 3, the latest software iteration for its Monarch robotically assisted bronchoscopy platform.
The clearance authorises the use of Dexter in ventral hernia repairs, a common US outpatient procedure.