AccessClosure, Inc. Launches MynxGrip™ Vascular Closure Device
New Grip Technology™ Sealant Redefines Active Closure
Mountain View, CA (February 27, 2012) – AccessClosure, Inc., the market leader in extravascular closure devices, announced today the FDA approval and US launch of the MynxGrip Vascular Closure Device (VCD). Built on the proven Mynx platform, the MynxGrip VCD offers an active, extravascular and patient-friendly vascular closure solution. MynxGrip adds the proprietary Grip Technology sealant to the distal end of the original Mynx Sealant.
AccessClosure, Inc. Marches to the Millionth Mynx!
AccessClosure, Inc. Marches to the Millionth Mynx!
Mountain View, California (September 28, 2011) – Mountain View, California (May 17, 2011) - AccessClosure, Inc., a leading manufacturer of extravascular closure devices, announced today the shipment of its one millionth Mynx unit. The Mynx Vascular Closure Device received its FDA approval in May 2007, following with its full commercial launch in September 2007. Physician feedback attributes the achievement of this monumental milestone to the fact that the Mynx sealant is extravascular, bio-inert and non-thrombogenic, while leaving nothing behind intra-arterially.
AccessClosure Signs Distribution Agreement to Enter Into UK, Switzerland and France
Growth of Mynx Device Continues in International Markets
Mountain View, California (May 17, 2011) – Mountain View, California (May 17, 2011)- AccessClosure, Inc., the market segment leader in extravascular closure devices, announced today an exclusive agreement with Biosensors International for the distribution of the Mynx™ Vascular Closure Device throughout the United Kingdom, Switzerland and France. The extravascular Mynx device, designed for patient comfort while providing hemostasis without sutures or implants, will be sold as part of Biosensors’ interventional cardiology product range.
Results from a Prospective, Randomized, Single-Site Study Indicate a Significant Reduction in Pain with the Mynx Vascular Closure Device versus Angio-Seal Device
Study Results Support Improved Patient Comfort with the Mynx Device
Mountain View, California (March 3, 2011) – AccessClosure, Inc., the U.S. market segment leader in extravascular closure devices, announced today results from the first published study* (Journal of NeuroInterventional Surgery) comparing the pain associated with deployment of different vascular closure devices (VCD) as the primary endpoint.
AccessClosure Announces Launch of New Mynx Cadence™ Vascular Closure Device
Enhanced Device Offers a Marked Advancement in Closure
AccessClosure Announces a Leadership Transition
Focused on Strategic Growth and Continued Commercial Leadership
AccessClosure Launches First True 5 French Vascular Closure Device
Mynx M5™ Offers Patients “Artery-Friendly” Closure Solution
