Peripheral Vascular

DABRA Laser System Yields 94% Success Rate in PAD Patients, Study Says

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DABRA Laser System Yields 94% Success Rate in PAD Patients, Study Says

Register to receive a free U.S. Market Report Suite for Peripheral Vascular Devices and Accessories – MedSuite report synopsis and brochure Ra Medical Systems, Inc. has announced that study results from Athar Ansari, MD, Director of the California Heart & Vascular Clinic. These results show a 94% success rate treating peripheral arterial disease using ablation on arterial

iData ResearchDABRA Laser System Yields 94% Success Rate in PAD Patients, Study Says
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Teleflex Announces FDA Premarket Approval of MANTA™ Vascular Closure Device

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Teleflex Announces FDA Premarket Approval of MANTA™ Vascular Closure Device

Register to receive a free U.S. Market Report Suite for Peripheral Vascular Devices and Accessories – MedSuite report synopsis and brochure Teleflex Inc. has announced its recent premarket approval (PMA) from the U.S. Food and Drug Administration for their MANTA™ Vascular Closure device. Teleflex is a global leader in medical technologies for surgery and critical care and

iData ResearchTeleflex Announces FDA Premarket Approval of MANTA™ Vascular Closure Device
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FDA Warns of Risks With Paclitaxel-Coated Balloons, Stents

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FDA Warns of Risks With Paclitaxel-Coated Balloons, Stents

Register to receive a free U.S. Market Report Suite for Peripheral Vascular Devices and Accessories – MedSuite report synopsis and brochure The U.S. Food and Drug Administration has released a warning letter to peripheral interventionalists and vascular medicine physicians regarding an increase in deaths involving paclitaxel-coated balloons and stents in a recent study. The notice outlines the

iData ResearchFDA Warns of Risks With Paclitaxel-Coated Balloons, Stents
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Micro Medical Solutions’ New MicroStent with 120 cm Delivery Catheter Receives CE Mark Approval

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Micro Medical Solutions’ New MicroStent with 120 cm Delivery Catheter Receives CE Mark Approval

Register to receive a free Europe Market Report Suite for Peripheral Vascular Devices and Accessories – MedSuite report synopsis and brochure Micro Medical Solutions (MMS), an innovator in the field of microvascular interventions designed to improve clinical outcomes and quality of life, announced that it has received CE Mark approval for a 4Fr.-compatible MicroStent 120 cm delivery

iData ResearchMicro Medical Solutions’ New MicroStent with 120 cm Delivery Catheter Receives CE Mark Approval
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Boston Scientific Announces Recommended Offer to Acquire BTG plc.

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Boston Scientific Announces Recommended Offer to Acquire BTG plc.

Register to receive a free U.S. Market Report Suite for Peripheral Vascular Devices and Accessories – MedSuite report synopsis and brochure Boston Scientific announced it has reached an agreement on the terms of a recommended offer to acquire BTG plc., a company headquartered in the United Kingdom, which develops and commercializes products used in minimally-invasive procedures targeting cancer

iData ResearchBoston Scientific Announces Recommended Offer to Acquire BTG plc.
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Medtronic Receives CE Mark Approval for the Valiant Navion(TM) Thoracic Stent Graft System

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Medtronic Receives CE Mark Approval for the Valiant Navion(TM) Thoracic Stent Graft System

Register to receive a free Europe Market Report Suite for Peripheral Vascular Devices and Accessories – MedSuite report synopsis and brochure Medtronic plc announced it has received CE Mark approval for the Valiant Navion(TM) thoracic stent graft system for the minimally invasive repair of all lesions of the descending thoracic aorta, including thoracic aortic aneurysms (TAA), blunt traumatic

iData ResearchMedtronic Receives CE Mark Approval for the Valiant Navion(TM) Thoracic Stent Graft System
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Medtronic Presents IN.PACT Global Study Three-Year Data

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Medtronic Presents IN.PACT Global Study Three-Year Data

Register to receive a free U.S. Market Report Suite for Peripheral Vascular Devices and Accessories – MedSuite report synopsis and brochure Medtronic plc data announced continue to reinforce the safety, durability, and consistency of the IN.PACT(TM) Admiral(TM) drug-coated balloon (DCB) in real-world patients with peripheral arterial disease (PAD). Three-year real-world results from the full clinical cohort of the

iData ResearchMedtronic Presents IN.PACT Global Study Three-Year Data
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Integer Receives FDA Approval for Thin Wall Radial Introducer Kit, RadialSeal(TM)

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Integer Receives FDA Approval for Thin Wall Radial Introducer Kit, RadialSeal(TM)

Register to receive a free U.S. Market Report Suite for Peripheral Vascular Devices and Accessories – MedSuite report synopsis and brochure Integer Holdings Corporation (“Integer”), a leading medical device outsource manufacturer, announced that it has received FDA and CE Mark approval for their new radial access introducer, RadialSeal(TM). The RadialSeal Introducer Kit is founded on Integer’s core

iData ResearchInteger Receives FDA Approval for Thin Wall Radial Introducer Kit, RadialSeal(TM)
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QT Vascular Enters Into Asset Purchase And Option Agreement With Teleflex

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QT Vascular Enters Into Asset Purchase And Option Agreement With Teleflex

Register to receive a free U.S. Market Report Suite for Peripheral Vascular Devices and Accessories – MedSuite report synopsis and brochure QT Vascular Ltd., (“QT Vascular“, and with its subsidiaries, the “Company“), announced that it has entered into an asset purchase and option agreement (the “APOA“) with Teleflex Life Sciences Unlimited Company and Teleflex Incorporated (“Teleflex“). Under

iData ResearchQT Vascular Enters Into Asset Purchase And Option Agreement With Teleflex
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Surmodics Announces FDA Clearance of a New .018” Low-Profile PTA Balloon Dilation Catheter

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Surmodics Announces FDA Clearance of a New .018” Low-Profile PTA Balloon Dilation Catheter

Register to receive a free U.S. Market Report Suite for Peripheral Vascular Devices and Accessories – MedSuite report synopsis and brochure Surmodics, Inc., a leading provider of medical device and in vitro diagnostic technologies to the healthcare industry, announced it received U.S. Food and Drug Administration (FDA) 510(k) clearance for its .018” Low-Profile percutaneous transluminal angioplasty (PTA)

iData ResearchSurmodics Announces FDA Clearance of a New .018” Low-Profile PTA Balloon Dilation Catheter
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