Boston Scientific’s Innovative Watchman left atrial appendage closure device, a proven alternative to anticoagulant drugs for patients in atrial fibrillation at high risk for stroke, has been implanted for the first time in Latin America.
CE Mark Approval
AIM Float for Sphere Medical Brings Near Real-Time Accurate Blood Gas Analysis Closer
Sphere Medical, a UK based developer of blood monitoring and diagnostic products, has issued a press release in which it has announced its flotation and new product plans.
STAAR Surgical Receives CE Mark Approval For Its Toric Collamer® IOL
CE Mark for Staar Surgical Allows Company to Expand its Presence in the Premium IOL Market in Europe with the nanoFLEX(TM) Toric IOL. First Shipments are Scheduled for Q1 2012
Gore Receives FDA Approval for Conformable GORE® TAG® Thoracic Endoprosthesis
Durable ePTFE Endoprosthesis Designed for Endovascular Repair of the Descending Thoracic Aorta Provides Conformability without Compromise
Vascular Designs’ IsoFlow™ Infusion Catheter Receives CE Mark Approval
Vascular Designs, Inc.has announced that its IsoFlow™ Infusion Catheter has received CE Mark approval for use in Europe and Canada
Transcatheter Cardiovascular Therapeutics conference 2011: Live link of UK case highlights FDA’s caution on Sapien Aortic Valve PMA.
Update from TCT2011 sourced from an article by Medical Device Daily
CE Mark for New Lead Enhances abiliti® Food Sensing/Gastric Stimulation System
IntraPace, Inc. has announced that it has received CE Mark for the LGL102, a new gastric stimulation/food sensing lead designed to work with the innovative abiliti(R) system, an implantable weight loss management system.
CE Mark for a New Embolic Protection System During TAVI
Claret Medical Announces CE Mark of a New Embolic Protection System to Address Stroke During Transcatheter Aortic Valve Intervention
ClearCount Announces First and Only CE Marked RFID-based Surgical Sponge System
ClearCount Medical Solutions has received approval to affix the CE mark to its SmartSponge and SmartWand-DTX products.
Abbott Receives U.S. FDA Approval for Next-Generation XIENCE PRIME™ Drug Eluting Stent
Following CE Mark approval in 2009, Abbott now gains FDA approval for Xience Prime Drug Eluting Stent
Apnex Medical, Inc. Receives CE Mark Approval for HGNS ® System to Treat Obstructive Sleep Apnea
Apnex Medical, Inc., has received CE Mark approval for its Hypoglossal Nerve Stimulation (HGNS®) System for use by people who suffer from obstructive sleep apnea.
SORIN Q3 RESULTS SHOW GROSS MARGINS ABOVE 60%
Sorin’s profits climbed by 47.5% year on year despite sales slowdown
Innocoll Announces European Approval for CollaGUARD®, Surgical Adhesion Barrier
Innocoll Inc. has announced the approval of CollaGUARD surgical adhesion barrier for the prevention of postoperative adhesions following abdominal and pelvic surgery.
SORIN GROUP LAUNCHES SONR® SENSOR BASED CARDIAC RESYNCHRONIZATION THERAPY (CRT) OPTIMIZATION SYSTEM
Sorin announced at the Venice Arrhythmias 2011 Congress, CE Mark approval and the European commercial launch of its innovative SonR CRT optimization system
Active Implants Announces CE Class III Medical Device Approval
Active Implants Corporation (AIC) today announced that it has received a CE Class III Certificate for its TriboFit® Hip System.
Onset Medical Receives European CE Mark Approval for the SoloPath Endovascular Access Catheter
Onset Medical Corporation announced today the Company has received CE Mark approval to begin marketing the Company’s SoloPathTM Endovascular Access Catheter in the European Union.