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 HSMN NewsFeed - 5 Nov 2024
Xeltis expands leadership team with appointment of Luc Verhees as Vice President of Clinical Business Development
Devices Personnel
 HSMN NewsFeed - 13 Jun 2024
Xeltis receives IDE approval from FDA for initiation of US pivotal trial for aXess(TM), its restorative vascular access conduit
Devices FDA
 HSMN NewsFeed - 28 Jun 2016
GORE(R) VIABAHN(R) Endoprosthesis Found to Provide Superior Patency and Reduced Interventions Versus Balloon Angioplasty Alone for Challenging AV Access Cases
Devices Interventional
 HSMN NewsFeed - 16 Mar 2015
Vascular Solutions Launches PolarCath(TM) Peripheral Dilatation System
Devices Interventional Product Launch
 HSMN NewsFeed - 19 Nov 2014
Argon Medical's CLEANER XT(TM) and CLEANER 15(TM) Rotational Thrombectomy Systems Receive FDA Clearance for Mechanical Declotting and Infusion in the Peripheral Vasculature
Devices Interventional FDA
 HSMN NewsFeed - 23 Apr 2014
The Medicines Company Adds Novel, Approved, Surgical Sealant to Its Surgical Hemostasis Portfolio
Devices Surgery Mergers & Acquisitions
 HSMN NewsFeed - 27 Mar 2014
CryoLife Acquires Distribution Rights and Purchase Option for ProCol(R) Vascular Bioprosthesis for Hemodialysis Access
Devices Distribution
 HSMN NewsFeed - 20 Feb 2014
Gore REVISE Clinical Study Demonstrates Superiority of GORE VIABAHN Endoprosthesis
Devices
 HSMN NewsFeed - 4 Apr 2013
CryoLife Receives FDA Clearance For Next Generation HeRO Device
Devices FDA
 HSMN NewsFeed - 15 Jan 2013
Rex Medical Cleaner15 Rotational Thrombectomy System Receives 510(k) Clearance
Devices Interventional Distribution FDA
 HSMN NewsFeed - 18 Jul 2012
Teleflex Acquires Hotspur Technologies, Inc.
Devices Interventional Mergers & Acquisitions
 HSMN NewsFeed - 15 May 2012
CryoLife to Acquire Hemosphere
Devices Mergers & Acquisitions
 HSMN NewsFeed - 6 Sep 2011
Hemosphere Receives CE Mark Approval for the HeRO(R) Graft
Devices Regulatory
 HSMN NewsFeed - 11 Mar 2010
Rex Medical Cleaner Rotational Thrombectomy System Receives 510(k) Clearance
Devices Interventional FDA
 HSMN NewsFeed - 10 Feb 2010
NEJM Publishes Trial Results Demonstrating Bard FLAIR(R) Endovascular Stent Graft is Superior to Balloon Angioplasty for Failing Dialysis Grafts
Devices Interventional
 HSMN NewsFeed - 1 Feb 2010
Pervasis Therapeutics Receives FDA Clearance for Pivotal Phase 3 Trial of Vascugel(R)
Biopharmaceuticals FDA
 HSMN NewsFeed - 13 Jul 2007
Gore REVISE Study Receives Conditional Approval from FDA
Devices Interventional FDA
 HSMN NewsFeed - 18 Jun 2007
Kensey Nash Announces Results of EU Coronary Study Using the Thromcat(TM) Thrombectomy Catheter System
Devices Interventional Cardiology
 HSMN NewsFeed - 11 Jun 2007
Gore AVIATOR Study Receives Conditional Approval from FDA
Devices Interventional FDA
 HSMN NewsFeed - 19 Mar 2007
Pervasis Therapeutics Launches Enrollment for Two Phase II Clinical Trials for Vascugel(TM)
Biopharmaceuticals Regenerative Medicine
 HSMN NewsFeed - 29 Nov 2006
FDA Clears Possis AngioJet(R) System for Blood Clot Removal in Veins
Devices FDA Interventional
 HSMN NewsFeed - 28 Sep 2006
OmniSonics Appoints Dr. Elvira Lang as Vice President and Chief Medical Officer
Devices Interventional Personnel
 HSMN NewsFeed - 27 Sep 2006
Pervasis Therapeutics' Vascugel(TM) Initiates U.S. Clinical Trials Following Successful FDA IND Review
Regenerative Medicine FDA
 HSMN NewsFeed - 24 Jul 2006
Kensey Nash Receives CE Mark Approval for QuickCat(TM) Extraction Catheter
Devices Regulatory Interventional
 HSMN NewsFeed - 28 Jun 2006
Journal of Invasive Cardiology Publishes New Results on Use of the Possis AngioJet(R) System in High-Risk Coronary Patients
Devices Interventional Cardiology
 HSMN NewsFeed - 31 May 2006
Thoratec Announces Completion of Enrollment in Bridge-to-Transplantation Arm of HeartMate(R) II Pivotal Trial
Devices Cardiology Surgery
 HSMN NewsFeed - 16 May 2006
Thoratec Receives FDA Approval of Continued Access Protocol for Bridge Arm of Its HeartMate(R) II Pivotal Trial
Devices Cardiology
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