NeuroOne® Accelerates Timeline of 510(k) Submission to FDA for the OneRF® Trigeminal Nerve Ablation System to Treat Facial Pain
Submission for New Intended Use That Leverages Company’s Patented OneRF® Technology Platform Expected in May 2025 EDEN PRAIRIE, Minn., March 11, ...
Medical Device Network on MSN5d
FDA grants 510(k) clearance to Zimmer’s new revision knee implant component
The US Food and Drug Administration (FDA) has granted 510(k) clearance to Zimmer Biomet's new revision knee implant component ...
Medical Device Network on MSN3d
FDA grants 510(k) clearance for J&J MedTech’s Monarch Quest
The US Food and Drug Administration (FDA) has granted 510(k) clearance for Johnson & Johnson (J&J) MedTech’s Monarch Quest ...
Endovascular Today2d
Perfuze Zipline Access Catheters Cleared by FDA
Perfuze, an Ireland-based developer of catheter-based aspiration technology for the treatment of acute ischemic stroke, ...
MassDevice2d
Spineart, eCential Robotics earn FDA nod for robotic-assisted spine surgery application
Spineart and eCential Robotics today announced the receipt of FDA 510(k) clearance for the use of an application for robotic ...
Endovascular Today1d
VentureMed Names Jordan Kepper as CMO and Announces Study Results for Flex VP System
VentureMed Group, Inc., a medical device company focused on arteriovenous access and peripheral arterial disease, recently ...
Yahoo Finance2d
Icon Energy Corp. (ICON)
After hours: March 14 at 7:59:56 PM EDT Loading Chart for ICON ...