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Medtronic advances Hugo robotic surgery system with new FDA filings and mesh clearance for hernia repair

Market News
03 Jun 2026
PRNewsWire
View Source
Bullish
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Medtronic announced key FDA submissions and clearance for its Hugo robotic-assisted surgery system, expanding its use to general and gynecologic surgeries in the U.S. The company filed 510(k) clearances for general surgery, gynecologic procedures, and the LigaSure RAS Maryland instrument, while receiving clearance for the ProGrip Advanced mesh for robotic ventral hernia repair. These developments broaden the system's clinical applications and support growing demand for robotic-assisted minimally invasive surgeries. Medtronic also completed enrollment in a clinical study evaluating the system's safety and effectiveness in gynecologic procedures, reinforcing its commitment to advancing surgical technology and patient care.

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