OrthAlign, Inc., the pioneer of handheld orthopedic navigation, today announced FDA 510(k) clearance for the Lantern ASC system, a solution that delivers the precision of advanced technology at a fraction of the cost and complexity of robotic systems. […]
Pixee Medical, a pioneer in Augmented Reality (AR) navigation for orthopedic surgery, today announced that it has received FDA 510(k) clearance for Knee+ NexSight, developed on a new AR platform for total knee arthroplasty (TKA). […]
Medivis, a pioneer in surgical intelligence, today announced it has received FDA 510(k) clearance for its Cranial Navigation platform – making it the world’s first augmented reality (AR) system cleared for intraoperative guidance in cranial neurosurgery. […]
Augmedics, a pioneer in augmented reality (AR) surgical navigation, today announced FDA 510(k) clearance of X2™, its next-generation AR headset for use with the xvision Spine System®. […]
Surgical Theater, the leader in surgical XR visualization, today announced U.S. Food and Drug Administration (FDA) 510(k) clearance for SyncAR® Spine, the next-generation release of its spine platform. This clearance expands the system’s capabilities with advanced XR tools powered by AI algorithms. […]
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 arthroplasty. This next-generation of AR was designed to address the fast-growing market of ambulatory surgical centers (ASCs). […]
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