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Searching News Database:  Surgical Hemostat 

 HSMN NewsFeed - 12 Aug 2021
Medcura raises $7.4 Million to Expand FDA-Approved Line of Hemostatic and Wound Treatment Products
Devices Surgery Venture Capital
 HSMN NewsFeed - 20 Aug 2015
Arch Therapeutics Appoints James Sulat to Board of Directors
Devices Surgery Personnel
 HSMN NewsFeed - 29 Apr 2014
CryoLife Receives FDA 510(k) Clearance for PerClot(R) Topical Hemostatic Powder in the U.S.
Devices FDA
 HSMN NewsFeed - 7 Nov 2013
BioCer Announces CE Approval for Mastectomy "Bra" plus FDA Approval for Hernia repair system TiO2Mesh(TM)
Devices Regulatory
 HSMN NewsFeed - 4 Sep 2013
Abyrx(TM), Inc. Receives FDA 510(k) Clearance for New Resorbable Hemostatic Bone Putty (Hemasorb Plus(TM))
Devices Surgery FDA
 HSMN NewsFeed - 19 Aug 2013
Bard Announces Agreement to Acquire Medafor, Inc.
Devices Surgery Mergers & Acquisitions
 HSMN NewsFeed - 8 Feb 2013
The Medicines Company and Bristol-Myers Squibb Begin Global Alliance for Recothrom(R)
Biopharmaceuticals Surgery Licensing Distribution
 HSMN NewsFeed - 12 Dec 2012
The Medicines Company and Bristol-Myers Squibb Agree to Global Alliance for Recothrom(R)
Biopharmaceuticals Licensing
 HSMN NewsFeed - 1 Jun 2011
ORTHOCON(R), Inc. Receives 510(k) Clearance to Market HEMASORB Apply
Devices Orthopaedic Surgery FDA
 HSMN NewsFeed - 16 May 2011
Orthovita, Inc. Agrees To Be Acquired by Stryker Corporation for $3.85 Per Share in Cash
Devices Mergers & Acquisitions
 HSMN NewsFeed - 11 Apr 2011
Orthovita Announces Presentation of Clinical Results Evaluating Vitagel(TM) Surgical Hemostat in Reducing Blood Loss During Primary Unilateral Total Knee Arthroplasty
Devices Orthopaedic Surgery
 HSMN NewsFeed - 4 Apr 2011
CryoLife Files Investigational Device Exemption (IDE) to Begin Clinical Trials for PerClot(R) in the U.S.
Devices Surgery FDA
 HSMN NewsFeed - 16 Feb 2011
Orthovita Launches Vitoss(TM) Bioactive Foam-2X Bone Graft Substitute at AAOS (American Academy of Orthopedic Surgeons) Meeting
Devices Orthopaedic
 HSMN NewsFeed - 10 Feb 2011
Orthovita Receives FDA Clearance for Vitoss(TM) Bimodal Bone Graft Substitute
Devices Orthopaedic Regenerative Medicine FDA
 HSMN NewsFeed - 7 Dec 2010
Orthovita Receives FDA Clearance for Vitoss(TM) Bioactive Foam-2X Bone Graft Substitute
Devices Orthopaedic FDA
 HSMN NewsFeed - 7 Oct 2010
CryoLife Receives Japanese Regulatory Approval for BioGlue Surgical Adhesive
Devices Surgery Regulatory
 HSMN NewsFeed - 6 Oct 2010
Orthovita Announces Presentation of Cortoss 24-Month Pivotal Study Results at the 25th Annual Meeting of the North American Spine Society
Devices Orthopaedic Neurosurgery
 HSMN NewsFeed - 4 Oct 2010
Orthovita Receives FDA Clearance for VITOMATRIX(TM) Bone Graft Substitute in Dental Applications
Devices Dental FDA
 HSMN NewsFeed - 10 Sep 2009
CryoLife Announces First Clinical Use of BioFoam(R)
Devices Surgery
 HSMN NewsFeed - 1 Apr 2009
Orthovita Submits Additional Data to FDA in Support of Its 510(k) Application for the Use of CORTOSS Bone Augmentation Material in Vertebral Augmentation
Devices Orthopaedic Neurosurgery FDA
 HSMN NewsFeed - 2 Dec 2008
Starch Medical Launches New, Bioinert Surgical Hemostats
Devices Surgery FDA
 HSMN NewsFeed - 1 Oct 2008
Haemacure Appoints Thomas J. Lynch, J.D., Ph.D. to Board of Directors
Devices Personnel
 HSMN NewsFeed - 22 Sep 2008
CryoLife Expands Distribution of Hemostase MPH(R) to Canada through Sorin Group Canada, Inc.
Devices Distribution
 HSMN NewsFeed - 22 Sep 2008
Orthovita Announces New VITOSS Bioactive Foam Pack Bone Graft Substitute
Devices Orthopaedic Neurosurgery
 HSMN NewsFeed - 15 May 2008
Haemacure appoints Reinaldo M. Diaz to its Board of Directors
Biopharmaceuticals Personnel
 HSMN NewsFeed - 17 Apr 2008
CryoLife to Distribute FDA-approved Hemostatic Agent Under Private Label
Devices Surgery Distribution
 HSMN NewsFeed - 14 Apr 2008
Orthovita Introduces VITASURE(TM) Absorbable Hemostat as Part of its Strategy to Leverage its Biomaterials Sales Organization
Devices Distribution
 HSMN NewsFeed - 15 Jan 2008
Orthovita Submits 510(k) Application to FDA for the Use of CORTOSS(R) Bone Augmentation Material in Vertebral Augmentation
Devices Orthopaedic Neurosurgery
 HSMN NewsFeed - 6 Aug 2007
Orthovita Receives CE Mark for VITAGEL(R) Surgical Hemostat and CELLPAKER(R) Plasma Collection System
Devices Regulatory
 HSMN NewsFeed - 21 Feb 2007
Orthovita Announces Completion of Patient Enrollment in Its U.S. Pivotal Clinical Study for the Use of CORTOSS(R) in the Treatment of Vertebral Compression Fractures
Devices Neurosurgery Orthopaedic
 HSMN NewsFeed - 7 Feb 2007
Orthovita Announces Appointment of Chief Business Officer and Chief Financial Officer
Devices Personnel
 HSMN NewsFeed - 5 Feb 2007
Orthovita Confirms That 510(k) Submission May Be Used to Seek Clearance for CORTOSS(R) Bone Augmentation Material for the Treatment of Vertebral Compression Fractures
Devices Orthopaedic Neurosurgery FDA
 HSMN NewsFeed - 22 Jan 2007
Surgeons to Witness Sea Change in Surgical Hemostasis at Annual STS Meeting
Devices Surgery
 HSMN NewsFeed - 22 Jan 2007
FDA Approves Orthovita's PMA Supplement for the CELLPAKER(R) Plasma Collection System Used in Conjunction with the VITAGEL(R) Surgical Hemostat
Devices FDA
 HSMN NewsFeed - 4 Dec 2006
Medafor's FlexiTip(TM) Applicator Facilitates Wound Access During Surgery
Devices Surgery
 HSMN NewsFeed - 8 Nov 2006
Orthovita Enters into Binding Letter of Intent to Purchase the VITAGEL(TM) Profit-Sharing Royalty Rights From Angiotech Pharmaceuticals (US), Inc.
Devices Licensing
 HSMN NewsFeed - 6 Nov 2006
OMRIX Biopharmaceuticals Submits Biologics License Application (BLA) for Human Thrombin Stand-Alone Product
Biopharmaceuticals
 HSMN NewsFeed - 9 Oct 2006
First U.S. Presentation of CORTOSS(R) IDE Pivotal Clinical Preliminary Data to Be Presented in a Poster at the Congress of Neurological Surgeons in Chicago
Devices Neurosurgery Orthopaedic
 HSMN NewsFeed - 3 Oct 2006
FDA Approves Medafor's Arista(TM) AH Absorbable Surgical Hemostat for U.S. Operating Rooms
Devices Surgery FDA
 HSMN NewsFeed - 14 Sep 2006
Orthovita Announces First Public Podium Presentation of CORTOSS(R) IDE Pivotal Clinical Data in the Treatment of Vertebral Compression Fractures at the European Society of Neuroradiology Meeting in Geneva
Devices Orthopaedic
 HSMN NewsFeed - 12 Sep 2006
Albert J. Pavucek, Jr. Joins Orthovita as Vice President Corporate Controller
Devices Personnel
 HSMN NewsFeed - 15 Aug 2006
Medafor, Inc., Announces the Introduction of MPatcH(R) Vascular Closure Device to International Cardiology Markets
Devices Interventional Cardiology
 HSMN NewsFeed - 16 Jun 2006
Orthovita Receives FDA Approval to Market Its VITAGEL(TM) Surgical Hemostat
Devices Surgery FDA
 HSMN NewsFeed - 1 May 2006
Two CORTOSS(R) Scientific Papers Will Be Presented at the 44th Annual Meeting of the American Society for Neuroradiology
Devices
 HSMN NewsFeed - 25 Apr 2006
Orthovita Expands Management Team with Addition of Christine J. Arasin as Vice President Business Development and Corporate Counsel
Devices Personnel
 HSMN NewsFeed - 17 Apr 2006
FDA Approves Further Changes To CORTOSS(R) IDE Pivotal Study Protocol
Devices Neurosurgery Orthopaedic FDA
 HSMN NewsFeed - 20 Mar 2006
Orthovita and Aastrom Biosciences Announce Collaboration Agreement for Orthopedic Products
Biopharmaceuticals Regenerative Medicine Orthopaedic
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