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Medical Devices & Biomaterials
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Date Item Title
07 Feb 2006 Dermisonics Develops Working Model of Antiseptic Wand
07 Feb 2006 NUCRYST Pharmaceuticals announces European approval for Acticoat™ Moisture Control
04 Feb 2006 MIV Therapeutics Executes Agreement to Collaborate on Future Drug Eluting Stent Technologies with Sahajanand
03 Feb 2006 OccuLogix Provides MIRA-1 Update
03 Feb 2006 Rafael Medical Technologies Receives Conditional IDE Approval For SafeFlo(R) Retrievable Vena Cava Filter Trial
02 Feb 2006 Novel Biodegradable Implant Leads the Way to the New Generation of Glaucoma Surgery - Anti Scarring Without the Fibroblast Inhibition
02 Feb 2006 DuraSeal(R) Sealant Receives CE Mark for Vascular Applications
01 Feb 2006 DUSA pharmaceuticals reports results from phase ii clinical trial for pdt of moderate to severe acne
01 Feb 2006 LDR Spine Secures FDA Approval to Conduct the First Clinical Second-Generation Cervical Artificial Disc-Mobi-C(R) Cervical Disc Prosthesis Approved for One and Two-Level Artificial Cervical Disc Clinical Trial in the U.S.; Patient Recruitment Now Underway
01 Feb 2006 Study Results Indicate the CYPHER Sirolimus-Eluting Coronary Stent May Reduce Re-Blockage and Chances of Major Side Effects in Patients with Complex Coronary Lesions
31 Jan 2006 Cytomedix Submits Application to FDA Seeking Marketing Clearance of Its AutoloGel System
31 Jan 2006 Guidant Receives European Approval for Drug Eluting Coronary Stent
25 Jan 2006 Guidant Receives Recommendation for Approval from European Competent Authority for Drug Eluting Stent
25 Jan 2006 Cytori Therapeutics Receives CE Mark for the Celution™ Stem Cell System; Achieves Condition for $11.0 Million Milestone Payment from Olympus Collaboration
25 Jan 2006 PolyNovo Announces a Global Partnering Deal
24 Jan 2006 INFUSE® Bone Graft/LT-Cage® Lumbar Tapered Fusion Device Approved For Use In Australia
24 Jan 2006 Kensey Nash Submits TriActiv FX(R) Embolic Protection System 510(k) Application to FDA
24 Jan 2006 Boston Scientific Announces Excellent Results in Study of Patients with Renal Artery Disease
24 Jan 2006 FDA Approves Updated Instructions for Use for the CYPHER® Sirolimus-Eluting Coronary Stent
23 Jan 2006 Artelon® implant for rotator cuff reinforcement receives clearance for marketing in the USA
09 Jan 2006 BioSyntech's BST-CarGel subject of prestigious publication
12 Dec 2005 Osteotech Receives Its Second Grafton(R) DBM 510(k) FDA Clearance
 
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