Pixee Medical, a pioneer in Augmented Reality (AR) navigation for orthopedic surgery, announces FDA 510(k) clearance of Knee+ NexSight, the cutting-edge AR guidance solution for total knee ...

BESANÇON, France--(BUSINESS WIRE)--Pixee Medical, a pioneer in Augmented Reality (AR) navigation for orthopedic surgery, announces FDA 510(k) clearance of Knee + NexSight, the cutting-edge AR guidance ...

Multi-Contact Probe Provides Alternative to Pharmaceutical and Invasive Surgical Treatments Submission Completed Earlier Than Anticipated EDEN PRAIRIE, Minn., April 23, 2025 (GLOBE NEWSWIRE) -- ...

Technologies has filed its 510(k) submission to the FDA for trigeminal nerve ablation earlier than previous guidance.

Medtronic (NYSE:MDT) announced today that it submitted 510(k) applications to the FDA seeking clearance for an interoperable ...

Medtronic has submitted 510(k) applications to the U.S. Food and Drug Administration seeking clearance for an interoperable pump.

Medtronic (MDT) has submitted 510(k) applications to the FDA seeking clearance for an interoperable pump. FDA clearance of this pump would pave ...

Receiving FDA clearance would allow Medtronic to pair its pumps with a glucose monitor being developed for the company by ...

Q1 2025 thrombectomy revenue reached $226.5 million, an increase of 20.7% year-over-year, with U.S. thrombectomy contributing significantly to this growth. International thrombectomy increased 3.3%, ...