Showing 1 to 25 of 126 Results
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W. L. Gore & Associates, Maker of GORE-TEX® Products, Marks 50 Years of Innovation
01 January 2008 - Company Founded in Family Basement Now Global Enterprise

Patient Enrollment Begins in Study on Efficacy of GORE SEAMGUARD® Staple Line Reinforcement for Circular Surgical Staplers
21 May 2007 - More than 2,500 colorectal implants of GORE SEAMGUARD® Bioabsorbable Staple Line Reinforcement for circular surgical staplers in past year

GORE DUALMESH® PLUS Biomaterial Inhibits Implant Infections by Drug-resistant 'superbugs® and Resists Biofilm Development
14 February 2007 - Hernia repair patch is the only to inhibit adherence of 10 different bacteria and resist initial biofilm formation for 14 days post-implantation

W. L. Gore & Associates Receives FDA Approval for Gore EMBOLDEN Clinical Study
09 October 2008 - Multi-center study will evaluate the safety and efficacy of the GORE Embolic Filter in conjunction with FDA-approved carotid stents

W. L. Gore & Associates takes on peripheral vascular disease at Vascular Interventional Advances (VIVA) Conference
11 October 2007 - W. L. Gore & Associates recently took part in the fifth annual Vascular Interventional Advances (VIVA) Conference in Las Vegas, where the focus was on new technologies for combating peripheral vascular disease (PVD), also called peripheral arterial disease (PAD).

W. L. Gore & Associates Announces Results of Gore EMPiRE Clinical Study
15 October 2008 - Study reports low major adverse event rates using the GORE Flow Reversal System

Gore Receives FDA Approval for Next Generation of Large Diameter GORE VIABAHN® Endoprosthesis with Heparin Bioactive Surface
21 July 2009 - Improved design now available with lower profile delivery system for use in iliac arteries.

FDA Approves GORE HELEX Septal Occluder for Treatment of Atrial Septal Defect
03 October 2007 - W. L. Gore & Associates today announced that the US Food & Drug Administration (FDA) granted approval for the GORE HELEX Septal Occluder with modified catheter delivery system indicated for the transcatheter closure of atrial septal defect (ASD).

Gore Receives FDA Approval for Modification of GORE VIABAHN® Endoprosthesis
17 September 2008 - Manufacturing modification of the only stent-graft approved for treatment of both iliac and superficial femoral arteries.

W. L. Gore & Associates Introduces GORE INFINIT Mesh - A Revolutionary Combination of Material and Structure
01 October 2008 - First and only 100% monofilament PTFE, large-pore knitted surgical mesh designed for long-term patient comfort and quality of life

W. L. Gore & Associates takes on peripheral vascular disease at Vascular Interventional Advances (VIVA) Conference
11 October 2007 - W. L. Gore & Associates recently took part in the fifth annual Vascular Interventional Advances (VIVA) Conference in Las Vegas, where the focus was on new technologies for combating peripheral vascular disease (PVD), also called peripheral arterial disease (PAD).

Gore Receives FDA Clearance for GORE BIO-A Fistula Plug
04 May 2009 - Combines Proven Synthetic Bioabsorbable Material with a Patented Design Engineered to Optimize Operative Success

GORE PRECLUDE® Vessel Guard Reduces Vascular Injury Risk Following Anterior Vertebral Surgery
07 May 2007 - W. L. Gore & Associates (Gore) announced today the availability of GORE PRECLUDE® Vessel Guard, the first non-biological membrane indicated as a cover for vessels following anterior vertebral surgery.

Gore Announces First Patient Enrolled in Gore REVISE Clinical Study
17 September 2008 - IDE Study to Compare Performance of GORE VIABAHN® Endoprosthesis with PROPATEN Bioactive Surface to Percutaneous Transluminal Angioplasty (PTA)

Gore Announces First Patient Treated with Recently-Cleared GORE Flow Reversal System
10 March 2009 - Breakthrough Gore system provides neuroprotection during carotid artery stenting by reversing blood flow at the treatment site

Rush University Medical Center First to Enroll Patient in the Gore REDUCE Clinical Study for the Indication of Patent Foramen Ovale (PFO) Closure
11 December 2008 - Multi-national trial to demonstrate safety, effectiveness of GORE HELEX Septal Occluder for PFO closure in patients with a history of cryptogenic stroke

First Patient Enrolled in Study of the GORE VIABAHN® Endoprosthesis with Heparin Bioactive Surface for Lower Limb Peripheral Vascular Disease
18 October 2007 - The first patient to enter a post-market evaluation designed to collect important data about the performance of the GORE VIABAHN® Endoprosthesis with Heparin Bioactive Surface in treating lower limb peripheral vascular disease (PVD), has undergone a successful implant.


Gore Recognized as One of World’s Most Innovative Companies
27 February 2009 - Company Earns a Spot on Fast Company’s 2009 "Fast 50" List

Gore Receives Approval from FDA for Unique Patent Foramen Ovale Stroke Study
05 May 2008 - Multinational trial randomizes stroke patients with Patent Foramen Ovale (PFO) to closure with the GORE HELEX Septal Occluder versus medical management

Gore Announces Broadened FDA Indication for GORE VIABAHN® Endoprosthesis for Iliac Occlusive Disease
17 September 2008 - Only Stent-Graft Approved for Treatment of Both Iliac and Superficial Femoral Arteries

England National Institute for Health Research Stroke Research Network Adopts Gore REDUCE Clinical Study
19 June 2012 - Study Investigates Device Closure of Patent Foramen Ovale (PFO) in Stroke Reduction.

GORE Flow Reversal System Cleared by FDA
09 February 2009 - Breakthrough system provides neuroprotection during carotid artery stenting by reversing blood flow at the treatment site and continuously directing emboli away from the brain

Gore Launches Study of Early TIPS Therapy for Ascites Patients
01 November 2010 - Experts Call for Fresh Look at Transjugular Intrahepatic Portosystemic Shunt (TIPS) Therapy for Liver Disease Patients

Gore REVISE Study Receives Approval From FDA
07 April 2008 - The Gore REVISE Study is a randomized, multi-center clinical trial intended to establish efficacy and safety of the GORE VIABAHN® Endoprosthesis with PROPATEN Bioactive Surface to revise arterio-venous grafts at the venous anastomosis in hemodialysis patients.

Gore receives FDA approval for GORE VIABAHN® Endoprosthesis with Heparin Bioactive Surface
05 September 2007 - Heparin-Bonded Endoprosthesis for Superficial Femoral Artery Interventions

Gore Announces New Configuration of GORE BIO-A® Tissue Reinforcement for Hiatal Hernia Repair
15 June 2008 - Gore adds thinner, more flexible, custom size bioabsorbable product

W. L. Gore & Associates Announce First Patient Enrolled in Gore EMBOLDEN Clinical Study
16 January 2009 - Multi-center study will evaluate safety and efficacy of the GORE Embolic Filter in carotid stenting for high risk surgical patients

Gore Reaffirms Commitment to Stroke Study, Launches Online Resource
15 November 2010 - Cardiology and Neurology Investigators Support Continued Study of Patent Foramen Ovale (PFO)

Gore Announces First Patient Enrolled in Gore REVISE Clinical Study
17 September 2008 - IDE Study to Compare Performance of GORE VIABAHN® Endoprosthesis with PROPATEN Bioactive Surface to Percutaneous Transluminal Angioplasty (PTA)

Gore Receives FDA Approval for Modification of GORE VIABAHN® Endoprosthesis
17 September 2008 - Manufacturing modification of the only stent-graft approved for treatment of both iliac and superficial femoral arteries.

GORE® Hybrid Vascular Graft Honored as Gold Winner in the 2012 Medical Design Excellence Awards
03 July 2012 - W. L. Gore & Associates (Gore) today announced that the GORE® Hybrid Vascular Graft was awarded Gold Winner in the Implant and Tissue-Replacement Products category of the 2012 Medical Design Excellence Awards (MDEA) competition.

Gore Receives CE Mark Approval for Removable GORE® VIABIL® Biliary Endoprosthesis
27 April 2010 - Expanded indication enables stent removal for up to 12 months following implantation for effective treatment of both malignant and benign biliary strictures.

Clinical Investigators Address Confusion Over Study of Patent Foramen Ovale (PFO) in Stroke Patients
13 December 2010 - W. L. Gore & Associates today released the following statement from the Gore REDUCE Clinical Study Principal Investigators on behalf of the Gore REDUCE Clinical Study Steering Committee in response to the recent CLOSURE I results presentation.

Gore Prevails in Heart Device Patent Infringement Suit
05 August 2013 - W. L. Gore & Associates (Gore) today announced a favorable ruling involving the GORE® HELEX® Septal Occluder.

Gore REVISE Study Receives Conditional Approval From FDA
12 July 2007 - Conditional approval to proceed with the Gore REVISE (VasculaR AccEss ReVision with GORE VIABAHN® EndoproSthesis vs PercutanEous Transluminal Angioplasty) Study was announced today by W. L. Gore & Associates.

Gore Receives FDA Approval for Conformable GORE® TAG® Thoracic Endoprosthesis
16 November 2011 - Durable ePTFE Endoprosthesis Designed for Endovascular Repair of the Descending Thoracic Aorta Provides Conformability without Compromise

Gore Recognizes Physicians as “Pioneers in Performance” for Exceptional Work in the Field of Endovascular Therapy
17 February 2009 - Leading practitioners and researchers from around the world commended for expanding treatment options for at-risk patients

Gore Receives CE Mark for New GORE® EXCLUDER® AAA Endoprosthesis Sizing Options
03 July 2012 - Broader Range of Sizes Now Accommodates More Patient Anatomies

Gore Receives Approval from FDA for Unique Patent Foramen Ovale Stroke Study
05 May 2008 - Multinational trial randomizes stroke patients with Patent Foramen Ovale (PFO) to closure with the GORE HELEX Septal Occluder versus medical management

Gore Receives FDA Approval for Innovative GORE® C3 Delivery System for GORE® EXCLUDER® AAA Endoprosthesis
04 January 2011 - New innovation enables physicians and interventionalists to reposition device for ideal placement in treating abdominal aortic aneurysms.

First Patient Enrolled in Gore® SCAFFOLD Clinical Study for Carotid Stenting
12 September 2013 - Pivotal Multicenter Investigational Study Begins at Medical University of South Carolina (MUSC), Evaluating Safety and Efficacy of Innovative GORE® Carotid Stent

First Patient Enrolled in Study Evaluating Performance of Spectranetics Laser Ablation Followed by GORE VIABAHN® Endoprosthesis with Heparin Bioactive Surface
25 February 2008 - Physician-sponsored study to examine combination therapy for lower limb in-stent restenosis in patients treated for Peripheral Vascular Disease.

Nominees Announced for 2011-2012 Pioneers in Performance Awards for the United States; Online Voting Opens at www.PioneersInPerformance.com
16 November 2011 - Awards Program Sponsored by W. L. Gore & Associates Honors Medical Specialists Advancing Therapy and Improving Patient and Clinical Performance Through Active Collaboration

Gore REVISE Study Receives Approval From FDA
07 April 2008 - The Gore REVISE Study is a randomized, multi-center clinical trial intended to establish efficacy and safety of the GORE VIABAHN® Endoprosthesis with PROPATEN Bioactive Surface to revise arterio-venous grafts at the venous anastomosis in hemodialysis patients.

Gore Receives CE Mark for GORE® Hybrid Vascular Graft
16 August 2012 - More than 2500 Successful Implants for Dialysis Access and Other Vascular Procedures

Rush University Medical Center First to Enroll Patient in the Gore REDUCE Clinical Study for the Indication of Patent Foramen Ovale (PFO) Closure
11 December 2008 - Multi-national trial to demonstrate safety, effectiveness of GORE HELEX Septal Occluder for PFO closure in patients with a history of cryptogenic stroke

Gore Reports First Patient Treated using GORE® C3 Delivery System for GORE® EXCLUDER® AAA Endoprosthesis
11 January 2011 - New medical innovation repositions the future of endovascular repair for abdominal aortic aneurysm

Gore Receives First FDA Approval for Endovascular Repair of Aortic Dissection
11 September 2013 - Conformable GORE® TAG® Thoracic Endoprosthesis First to Receive Indication for Aneurysm, Trauma and Dissection

Gore Receives CE Mark for GORE PRECLUDE® Vessel Guard
06 May 2008 - Distinguished seal allows biomaterial to be used across the European Union

New GORE® EXCLUDER® AAA Endoprosthesis Sizing Options Available
29 November 2011 - Broader Range of Sizes Now Accommodates More Patient Anatomies

Gore Provides Update on Patent Foramen Ovale (PFO) Stroke Study
08 July 2010 - Gore Reaffirms Commitment to Multi-National, Randomized Study on PFO Closure in Stroke Patients using GORE® HELEX Septal Occluder Versus Medical Management

Gore REVISE Study Receives Conditional Approval From FDA
12 July 2007 - Conditional approval to proceed with the Gore REVISE (VasculaR AccEss ReVision with GORE VIABAHN® EndoproSthesis vs PercutanEous Transluminal Angioplasty) Study was announced today by W. L. Gore & Associates.

Gore Presents Astronaut and Scientist Mae C. Jemison, MD, as Keynote Speaker at Women in Vascular Leadership Luncheon
18 March 2014 - The pioneering Dr. Jemison, who flew aboard the Space Shuttle Endeavour, will address vascular surgeons at the 2014 SCVS symposium in Carlsbad, Calif.

First Patient Enrolled in GORE® Septal Occluder Clinical Study for Atrial Septal Defect
19 October 2012 - Pivotal Multicenter Trial Begins at Duke University, Evaluating Safety and Efficacy of Innovative ASD Closure Device

Endovascular Repair of Descending Thoracic Aortic Aneurysm
25 October 2007 - On November 6, 2007, at 3 pm (EST) surgeons and radiologists from the University of Michigan Health System will perform a descending thoracic aortic aneurysm repair with the GORE TAG® Thoracic Endoprosthesis.

New Clinical Evidence Supporting Efficacy of GORE® PROPATEN® Vascular Graft
19 January 2011 - Jes Lindholt, MD, PhD presented new study data from a Scandinavian clinical trial designed to compare patency rates of the GORE PROPATEN Vascular Graft with standard ePTFE grafts (GORE-TEX® Stretch Vascular Graft).

Gore Receives FDA Approval for 25 cm GORE® VIABAHN® Endoprosthesis
06 November 2013 - Longest stent-graft introduced in the United States

Gore Receives CE Mark for GORE VIABAHN® Endoprosthesis with PROPATEN Bioactive Surface
14 December 2008 - Gore’s proprietary heparin surface has proven valuable in the clinical treatment of arterial vascular disease.

Gore Receives First FDA Approval for Endovascular Repair of Traumatic Aortic Transections
19 January 2012 -

Conformable GORE® TAG® Thoracic Endoprosthesis Designed for Endovascular Repair of the Descending Thoracic Aorta Provides Conformability without Compromise


Gore Launches Improved GORE® HELEX Delivery System in Europe
12 July 2010 - W. L. Gore & Associates is pleased to announce the availability of an improved iteration of the GORE® HELEX Septal Occluder. The rollout of the improvement will begin in Europe immediately, and its availability will open up to other markets pending respective regulatory approvals.

W. L. Gore & Associates Presents New Data and Clinical Updates at Transcatheter Cardiovascular Therapeutics (TCT) Conference 2008
08 October 2008 - Gore continues commitment to clinical research with symposia, ongoing clinical studies and emerging technologies



Gore Receives Approval to Market GORE TAG® Thoracic Endoprosthesis in Japan
03 June 2008 - Expedited Clearance Provides Less Invasive Treatment Alternative for Thoracic Aortic Aneurysms

Gore Receives FDA Approval for New GORE® EXCLUDER® AAA Endoprosthesis Components
14 January 2013 - Expanded Treatment Options for Abdominal Aortic Aneurysms Provide More Patients with Access to Minimally Invasive Endovascular Repair

Gore Receives Health Canada Approval for Removable GORE® VIABIL® Biliary Endoprosthesis
17 January 2011 - New treatment option now available for benign and malignant biliary strictures

GORE® EXCLUDER® Iliac Branch Endoprosthesis Is First Dedicated System of Its Kind Approved in Europe
07 November 2013 -

First Successful Implants Completed in Italy and the United Kingdom, Providing Endovascular Repair to Iliac Arteries


Gore receives FDA approval for GORE VIABAHN® Endoprosthesis with Heparin Bioactive Surface
05 September 2007 - Heparin-Bonded Endoprosthesis for Superficial Femoral Artery Interventions

W. L. GORE & ASSOCIATES NAMED A TOP U.S. WORKPLACE
19 January 2012 - Company has appeared in every listing of the "100 Best Companies to Work For"

Doctors in New South Wales and Victoria Become First in Australia to Treat Patients with Aortic Aneurysms Using GORE® DrySeal Sheath
03 August 2010 - Revolutionary Device Delivers Consistent Performance, Better Control, and Minimized Blood Loss During Minimally Invasive Endovascular Procedure

Vascular Surgeons Present Positive Study Results for the GORE PROPATEN® Vascular Graft and Updates to the GORE VIABAHN® Endoprosthesis
17 September 2009 - Physicians report new information at the Society for Vascular Surgery's annual meeting


Gore Reacts to RESPECT Trial Results
26 October 2012 - Data Calls for Further Research on Transcatheter Patent Foramen Ovale (PFO) Closure

Endovascular Repair of Descending Thoracic Aortic Aneurysm
26 October 2007 - Heart Disease: On Nov 16th, 2007, see a live endovascular repair of a descending thoracic aortic aneurysm with the GORE TAG® Thoracic Endoprosthesis. Michael D. Dake, MD, Professor of Radiology, Internal Medicine, Surgery and Chairman of the UVA Department of Radiology will host this live broadcast.

Improved GORE® DrySeal Sheath with Hydrophilic Coating Launches in Europe
23 January 2013 - New Product Engineered to Increase Sheath Lubricity, Minimize Coating Particulation for Easier Insertion and Removal in Treating Patients with AAA and TAA

Gore Announces European Availability of Next Evolution of GORE® VIABAHN® Endoprosthesis
19 January 2011 - Lower profile delivery system in Europe provides more options for endoluminal bypass

First Patient Enrolled in Gore EXCLUDER Iliac Branch Study
14 November 2013 - Multi-Center Study to Assess Safety and Effectiveness of GORE® EXCLUDER® Iliac Branch Endoprosthesis for Treatment of Common Iliac Artery Aneurysms (CIAA) or Aorto-Iliac Aneurysms (AIA).

Gore Announces Broadened FDA Indication for GORE VIABAHN® Endoprosthesis for Iliac Occlusive Disease
17 September 2008 - Only Stent-Graft Approved for Treatment of Both Iliac and Superficial Femoral Arteries

Gore Recognizes Physicians as “Pioneers in Performance” for Exceptional Work in the Field of Endovascular Therapy
17 February 2009 - Leading practitioners and researchers from around the world commended for expanding treatment options for at-risk patients

Gore Joins Vascular and Endovascular Leaders in Honoring 2012 Pioneers in Performance in Europe
16 April 2012 - Leading Practitioners and Researchers from Europe Commended for Expanding Treatment Options for At-Risk Patients

First Patient Implanted in Investigational Study for Self Sealing GORE® ACUSEAL Vascular Graft
12 August 2010 - Study Gauges Benefits for End Stage Renal Disease Patients During Hemodialysis

Gore Joins Vascular and Endovascular Physicians in Honoring 2013 Pioneers in Performance Winners for Latin America
29 April 2013 - Leading Practitioners and Researchers from Mexico, Central and South America CICE 2013

Gore Showcases New Endovascular Repair Simulation Technology at VIVA
18 October 2011 - Physicians Simulate Real Patient Cases Ushering New Era of Procedure Preparation

Gore Receives FDA Approval for Next Generation of Large Diameter GORE VIABAHN® Endoprosthesis with Heparin Bioactive Surface
21 July 2009 - Improved design now available with lower profile delivery system for use in iliac arteries.

Gore Joins Vascular and Endovascular Leaders in Recognizing the 2014 Pioneers in Performance for North America
19 November 2014 - Leading Practitioners and Researchers from North America Commended for Commitment to Advancing Vascular and Endovascular Therapy

New 10 cm GORE® Hybrid Vascular Graft Delivers Unprecedented Versatility
14 November 2012 - Increased Length of Nitinol Reinforced Section Allows for Access to Deeper Vessels, Extends Landing-Zone Positioning Options

Gore Announces First Implant of Next Generation Conformable GORE TAG® Thoracic Endoprosthesis in US Clinical Trial for the Treatment of Thoracic Aortic Aneurysms
20 October 2009 - W. L. Gore & Associates (Gore) today announced the first human implants of the next generation Conformable GORE TAG® Thoracic Endoprosthesis for the treatment of thoracic aortic aneurysms (TAAs)

W. L. Gore & Associates Named a Top U.S. Workplace
16 January 2013 - Company has appeared in every listing of the “100 Best Companies to Work For”

First Australian Patients Enrolled in Gore Global Registry for Endovascular Aortic Treatment
20 March 2012 - Royal Prince Alfred Hospital First in Australia


Gore Announces FDA Approval of Next Evolution of GORE® VIABAHN® Endoprosthesis
17 February 2011 - Lower profile delivery system in the US provides more options for endoluminal bypass

Gore Launches Early Cannulation Capable GORE® ACUSEAL Vascular Graft
19 November 2013 - Results of early cannulation clinical trial presented at the 2013 VEITHsymposium

W. L. GORE & Associates Named a Top U.S. Workplace
16 January 2014 - Company has appeared in every listing of the “100 Best Companies to Work For”

VIBRANT Study of GORE VIABAHN® Endoprosthesis Completes Enrollment
01 January 2008 - Randomized Trial to Assess Patency of Covered Stents vs. Nitinol Stents for the Treatment of Vascular Disease

Gore REVISE Study Receives Approval From FDA
07 April 2008 - The Gore REVISE Study is a randomized, multi-center clinical trial intended to establish efficacy and safety of the GORE VIABAHN® Endoprosthesis with PROPATEN Bioactive Surface to revise arterio-venous grafts at the venous anastomosis in hemodialysis patients.

SVS and Gore Support Increasing Numbers of Women in Vascular Surgery
23 May 2012 - Women’s Leadership to Take Spotlight at the Society for Vascular Surgery 2012 Vascular Annual Meeting


Gore Medical Receives National Honor for Operational Excellence
20 June 2013 - W. L. Gore & Associates named as a winner of the eighth annual Pinnacle Award

Gore Acquires Intellectual Property of NMT Medical, Inc.
19 October 2011 - CLOSURE I Trial Data May Create Better Clinical Understanding of Patent Foramen Ovale (PFO) in Stroke Patients

W. L. Gore & Associates takes on peripheral vascular disease at Vascular Interventional Advances (VIVA) Conference
11 October 2007 - W. L. Gore & Associates recently took part in the fifth annual Vascular Interventional Advances (VIVA) Conference in Las Vegas, where the focus was on new technologies for combating peripheral vascular disease (PVD), also called peripheral arterial disease (PAD).

Gore and AAAneurysm Outreach Partner to Increase Early Detection of Abdominal Aortic Aneurysm (AAA)
28 January 2014 - New Campaign Will Employ Awareness, Community Outreach, and Patient Screening to Fight AAA

Gore REDUCE Clinical Study Principal Investigators Respond to Recent RESPECT Clinical Trial and PC Trial Results
15 November 2012 - Gore REDUCE Clinical Study Investigators Implored to Continue Enrollment, Drive 'Diligent Continuation of Study'

W. L. Gore & Associates enrolls first patient in study of 45 mm GORE TAG® Thoracic Endoprosthesis
20 February 2007 - W. L. Gore & Associates announced today that the first patient has been enrolled in a US Food and Drug Administration (FDA) approved IDE study for the 45 mm* GORE TAG® Thoracic Endoprosthesis for treatment of aneurysms of the descending thoracic aorta.

Gore Launches Lower Profile GORE® EXCLUDER® AAA Endoprosthesis Contralateral Leg Components in US and Europe
11 March 2013 - Addition to Series of Reduced Profile GORE® EXCLUDER® Devices Launching This Year

GORE® Hybrid Vascular Graft Commercially Available in the United States
01 June 2011 - W. L. Gore & Associates today is announcing commercial availability in the US of the GORE® Hybrid Vascular Graft.

Nominees Announced for 2011 Pioneers in Performance Awards for Europe; Online Voting Opens at www.PioneersInPerformance.com
11 April 2011 - Awards Program Sponsored by W. L. Gore & Associates Honors Medical Specialists Advancing Therapy and Improving Patient and Clinical Performance Through Active Collaboration

Gore Receives CE Mark for GORE® PROPATEN® Vascular Graft for Hemodialysis Access
22 February 2011 - Unique Vascular Graft Transcends Mechanical Solutions for Dialysis Access

GORE® C3 Delivery System Approved In Japan
03 December 2013 - System Enables Physicians and Interventionalists to Reposition GORE® EXCLUDER® AAA Endoprosthesis for Ideal Placement in Treating Abdominal Aortic Aneurysms


First Patient Enrolled in Study of the GORE VIABAHN® Endoprosthesis with Heparin Bioactive Surface for Lower Limb Peripheral Vascular Disease
18 October 2007 - The first patient to enter a post-market evaluation designed to collect important data about the performance of the GORE VIABAHN® Endoprosthesis with Heparin Bioactive Surface in treating lower limb peripheral vascular disease (PVD), has undergone a successful implant.

Gore REVISE Study Receives Conditional Approval From FDA
12 July 2007 - Conditional approval to proceed with the Gore REVISE (VasculaR AccEss ReVision with GORE VIABAHN® EndoproSthesis vs PercutanEous Transluminal Angioplasty) Study was announced today by W. L. Gore & Associates.

Gore Participates in FDA Circulatory System Devices Advisory Panel Meeting
07 June 2012 - Focus on Safety and Effectiveness of GORE® HELEX® Septal Occluder for Closure of Atrial Septal Defect (ASD)

Gore Delivers New Choice for Complex Soft Tissue Reinforcement
04 October 2010 - Economical Alternative to Biologics, Now In Larger Sizes

GORE® Septal Occluder Honored as Best In Show and Gold Winner in the 2013 Medical Design Excellence Awards
26 June 2013 - Recognition for Innovation in Expanding Treatment Options for Patients

Royal Sussex County Hospital First in the UK to Enroll a Patient in the Gore REDUCE Clinical Study for the Indication of Patent Foramen Ovale (PFO) Closure
01 November 2011 - International study to demonstrate safety, effectiveness of GORE® HELEX® Septal Occluder for PFO closure in patients with a history of cryptogenic stroke

Gore Receives CE Mark for Longer Length GORE® VIABAHN® Endoprosthesis
01 July 2010 - Longest stent-graft ever introduced in Europe for SFA endoluminal bypass

Gore REVISE Clinical Study Demonstrates Superiority of GORE VIABAHN Endoprosthesis
20 February 2014 - GORE Device Outperforms Standard Treatment Option for Stenoses or Thrombotic Occlusions

Improved GORE® DrySeal Sheath with Hydrophilic Coating Allows for Smooth and Minimally Invasive Endovascular Repair
18 December 2012 - Engineered to Increase Sheath Lubricity and Minimize Coating Particulation for Easier Insertion and Removal in Treatment of Patients with AAA and TAA

Gore Receives European CE Mark Approval for Next Generation Conformable GORE TAG® Thoracic Endoprosthesis
07 November 2009 - First human implant highlights innovative, conformable design of GORE TAG® Thoracic Endoprosthesis

Nominees Announced for 2013-2014 Pioneers in Performance Awards for Europe; Online Voting Opens at PioneersInPerformance.com
06 April 2013 -

Awards Program Sponsored by W. L. Gore & Associates Honors Medical Specialists Advancing Therapy and Improving Patient and Clinical Performance Through Active Collaboration


Gore Receives Zero Reports of Erosion Associated With GORE® HELEX® Septal Occluder
22 August 2011 - W. L. Gore & Associates (Gore) today reported that it has received zero accounts of erosion of the aortic root or the free wall of the atrium associated with the worldwide use of the GORE® HELEX® Septal Occluder.

First Patient Enrolled in Gore Early TIPS for Ascites Study at Indiana University Hospital
25 April 2011 - Clinical Study to Examine Effects of Early Intervention with Transjugular Intrahepatic Portosystemic Shunt (TIPS) Therapy on Transplant-Free Liver Disease Survival Rates


FDA Approves GORE® VIABAHN® Endoprosthesis for Revision of the Arteriovenous Access
11 December 2013 - Flexibility and Durability to Aid Hemodialysis Patients

First Patient Enrolled in Gore TAG Thoracic Branch Endoprosthesis LSA Feasibility Study
27 January 2014 - Multi-Center Study to Assess Feasibility of Gore Device to Treat Historically Challenging Patient Population

Showing 1 to 25 of 126 Results
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