Key facts
- Medtronic submitted 510(k) filings for Hugo robotic-assisted surgery system expansion into general and gynecologic specialties in the US.
- A 510(k) filing is pending for the LigaSure™ RAS Maryland instrument on the Hugo RAS system.
- Medtronic received 510(k) clearance for ProGrip™ Advanced self-gripping polypropylene mesh for robotic-assisted ventral hernia repair surgeries.
- The ProGrip™ mesh is cleared for use with the Hugo RAS system.
Medtronic plc, a global medical technology company, announced on June 3, 2026, that it has submitted 510(k) filings to expand the use of its Hugo™ robotic-assisted surgery system into general and gynecologic specialties within the United States. Concurrently, the company announced that a 510(k) filing is pending for the LigaSure™ RAS Maryland instrument, designed for use with the Hugo RAS system. Additionally, Medtronic has received 510(k) clearance for its ProGrip™ Advanced self-gripping polypropylene mesh, which is intended for use in robotic-assisted ventral hernia repair surgeries utilizing the Hugo RAS system.