MedTech News
Momentis Surgical Receives FDA 510(k) Clearance for Second Generation Anovo® Robotic Platform, Introducing Haptic Feedback and Dual-Mode Articulation
TEL AVIV, Israel and FORT LAUDERDALE, Fla., Nov. 11, 2024 /PRNewswire/ — Momentis Surgical Ltd., a leader in robotic-assisted surgical innovation, today announced the U.S. Food and Drug Administration (FDA) 510(k) clearance for its second-generation Anovo® robotic surgical platform.
Avanos Medical earns Medicare win for infusion pump tech
Avanos Medical announced today that a Centers for Medicare and Medicaid Services (CMS) payment rule benefits its infusion systems.
Pumping the brakes on dangerous proteins
RNA in the human genome’s understudied ‘Wild West’ might be key to regulating genetic disorders like epilepsy, autism
Johnson & Johnson MedTech Receives FDA Approval for the VARIPULSE™ Pulsed Field Ablation Platform for the Treatment of Atrial Fibrillation
IRVINE, Calif., Nov. 7, 2024 /PRNewswire/ — Johnson & Johnson MedTech, a global leader in cardiac arrhythmia treatment, today announced the U.S. Food & Drug Administration (FDA) approval of the VARIPULSE™ Platform for the treatment of drug refractory paroxysmal Atrial Fibrillation (AFib).
Corin wins FDA clearance for new femoral stem
Corin announced that it received FDA 510(k) clearance for its Icona femoral stem implant for total hip arthroplasty (THA).
Startup gives surgeons a real-time view of breast cancer during surgery
The drug-device combination developed by MIT spinout Lumicell is poised to reduce repeat surgeries and ensure more complete tumor removal.
New haptic patch transmits complexity of touch to the skin
Device delivers various sensations, including vibrations, pressure and twisting
Zeta Surgical® AI-Powered Navigation System Receives FDA Special 510(k) Clearance for Expanded Indications and Instrument Compatibility
BOSTON, Nov. 6, 2024 /PRNewswire/ — Zeta Surgical announced today that its Zeta Navigation System has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for use with expanded instruments and enhanced hospital connectivity.