Eximo Medical Ltd. says it has received U.S. FDA 510(k) clearance for its B-Laser™ Atherectomy System for Peripheral Artery Disease (PAD)
Approval/Clearance
Clearance and Launch for Mentor’s CPX4 Smooth Breast Tissue Expander
New tissue expander with smooth surface aids insertion and removal in breast reconstruction surgery
FDA Clearance Expands Scalp Cooler Indication
Experts welcome expansion of indication to include solid tumour patients
FDA Clears Expanded Indication of Acclarent AERA® Eustachian Tube Balloon Dilation System
Procedures may now be performed on patients as young as 18. New data on local anesthesia also recognized
Strong U.S. Sales Growth for joimax®: Now Company Launches MultiZYTE® Facet and SI Joint Treatment Set
joimax has also obtained full approval of its Endovapor® 2 system in China
FDA Clearance for MedShape DynaNail XL
New 260mm and 300mm offerings expand indications for NiTiNOL-based TTC Fusion device
Radar Breast Tumor Localization Gets FDA Clearance for Long Term Implant
Cianna Medical’s SCOUT system uses highly sophisticated radar technology for unprecedented precision
Abbott’s MitraClip First Transcatheter Mitral Valve Repair Device Approved in Japan
Japanese study data underpins approval
FDA Clears Stryker Cementless Mako Total Knee with Triathlon® Tritanium®
Stryker aims to strengthen its leadership position in robotic technology
FDA Clears K2M’s YUKON™ OCT Spinal System
Next-generation occipito-cervico-thoracic fusion system features an advanced polyaxial screw for degenerative & complex spinal pathologies
Pentax Medical Europe Unveils Unique Duodenoscope with Disposable Elevator Cap
CE mark for Pentax Medical’s DEC™ Duodenoscope delivers clinicians a unique solution for enhancing infection prevention and improving reprocessing efficiency, says company
FDA Approval and U.S. Launch of Medtronic’s New Chronic Intractable Pain Platform
Intellis includes the world’s smallest implantable spinal cord stimulator
U.S. 510(K) Clearance for Adherium’s Smartinhaler for AstraZeneca’s Symbicort Aerosol
Data show improved adherence by up to 59% in adults and 180% in children
CE Mark and EU Launch of MyoVista® High Sensitivity ECG Device
Low-Cost cardiac screening advancement aims to improve early detection of heart disease
FDA Clears COALESCE™ Porous PEEK Lumbar Interbody Fusion Device
Material benefits said to include improved biologic fusion and biomechanics
FDA Clearance for “Game Changing” Cardiologs ECG Analysis Platform
Cloud-based “AI” cardiac monitoring-analysis web service gets U.S. go ahead