Regulatory

CE Mark approval was granted for the 7D Surgical Cranial Module and Percutaneous Spine Module.

RBknee is an AI-based analysis tool aimed at improving the efficiency and accuracy of radiographic knee osteoarthritis diagnosis.

The clearance includes the pre-surgery patient-specific planning software and 3D-printed cutting guides for the QUANTUM Total Ankle.

ROSA Hip and ONE Planner Hip complement current robotic solutions for total and partial knee replacement.

NuVasive announced the commercial launch of Pulse, which is now available for sale in targeted global regions.

ARVIS is the first wearable surgical navigation system to be cleared for both hip and knee arthroplasty.

Pulse is designed to increase efficiency and procedural reproducibility, while addressing common clinical challenges in spine surgery.

Micromate, available in the U.S. spine fusion landscape through partner company Fusion Robotics, can perform almost every non-invasive image-guided procedure.

Vuzix announced the market expansion to support the NextAR surgical augmented reality platform developed by Medacta.

Medacta's knee, shoulder and spine applications received CE Mark approval, and its shoulder application obtained FDA 510(k) clearance.