News
Ethicon Launches Next Generation Energy Device at American Society of Colon and Rectal Surgeons’ Annual Meeting
April 25, 2013 8:30 am | by The Associated Press | CommentsTo expand choice and help surgeons provide greater precision, Ethicon Endo-Surgery, Inc. today announces the launch of the HARMONIC ACE + Shears with Adaptive Tissue Technology (HARMONIC ACE + Shears), the next generation product in the best-in-class HARMONIC portfolio of ultrasonic surgical devices that can handle multiple surgical jobs
A*STAR and Veredus Laboratories Create Market's First Lab-on-Chip for the Detection of Multiple Tropical Infectious Diseases
April 25, 2013 3:01 am | by The Associated Press | CommentsThe Agency for Science, Technology and Research (A*STAR) and Veredus Laboratories, a leading supplier of innovative molecular diagnostic tools, announced the launch of VereTrop, the first biochip in the molecular diagnostics market that can identify 13 different major tropical diseases from...
Profound Medical Announces Initiation of TULSA Clinical Trial for Treatment of Localized Prostate Cancer
April 25, 2013 12:01 am | by PR Newswire | CommentsProfound Medical Inc. today announced the commencement of its Health Canada approved, multi-center TULSA clinical trial for its minimally invasive, novel ablation device used to facilitate prostate cancer treatment. In the world's first procedure of its kind, a patient was treated in a collaborative effort with London Health Sciences Center...
Meeting Announcement: July 24-25, 2013 Orthopaedic and Rehabilitation Devices Panel of the Medical Devices Advisory Committee
April 25, 2013 12:00 am | by U.S. Food & Drug Administration | CommentsOn July 24, 2013, the committee will discuss, make recommendations, and vote on information related to the premarket approval application for the Kineflex/C Cervical Artificial Disc sponsored by SpinalMotion. The Kineflex/C is a metal-on-metal (cobalt chrome molybdenum alloy) cervical total disc replacement device.
510(k) Device Modifications: Deciding When to Submit a 510(k) for a Change to an Existing Device, May 17, 2013
April 25, 2013 12:00 am | by U.S. Food & Drug Administration | CommentsThe purpose of the meeting is to discuss FDA’s past, present, and future policy on 510(k) Modifications with external stakeholders. FDA seeks comment from stakeholders on different options, both in the form of submissions to the docket for the Federal Register notice associated with this meeting and in discussion during the public meeting.
Under the Skin, a Tiny Laboratory
April 24, 2013 9:55 pm | by I-Micronews | CommentsHumans are veritable chemical factories - we manufacture thousands of substances and transport them, via our blood, throughout our bodies. Some of these substances can be used as indicators of our health status. A team of EPFL scientists has developed a tiny device that can analyze the concentration of these substances in the blood.
Ergoresearch to Acquire Victhom
April 24, 2013 5:21 pm | by PR Newswire | CommentsErgoresearch Ltd. and Victhom Human Bionics Inc. announced today that the Superior Court of Québec has issued a final order approving the previously-announced plan of arrangement relating to the acquisition by Ergoresearch Inc., a direct wholly-owned subsidiary of Ergoresearch, of Victhom.
Eastman Expands Non-Phthalate Plasticizer Portfolio
April 24, 2013 5:10 pm | by Eastman Chemical Company | CommentsEastman Chemical Company has announced it will expand its non-phthalate plasticizer portfolio with the addition of Eastman 168™ SG (sensitive grade) non-phthalate plasticizer. Eastman 168 SG non-phthalate plasticizer is an enhanced grade of the Eastman 168 non-phthalate plasticizer.
Medstrat Posts Documents Confirming Terms Of Dismissal Of Merge's Lawsuit
April 24, 2013 4:53 pm | by PR Newswire | CommentsMedstrat, Inc., a leading provider of picture archiving and communications system (PACS) technology to Orthopaedic practices and hospital systems, announced today that it has posted the terms of the Settlement Agreement by which Merge Healthcare dismissed its November 14, 2012 lawsuit filed against Medstrat.
Potential for Delivery System Catheter Separation Prompts Cook Medical To Initiate Voluntary Global Recall of Zilver® PTX® Drug Eluting Stent
April 24, 2013 4:40 pm | by The Associated Press | CommentsBased on its investigation into a small number of complaints that the delivery system of the device had separated at the tip of the inner catheter, Cook Medical has initiated a nationwide/global voluntary recall of its Zilver® PTX® Drug Eluting Peripheral Stent.
Life Care Medical Devices Ltd Announces CE Mark And Planned Commercialization For Laparoscopic Surgery Access Device
April 24, 2013 4:29 pm | by The Associated Press | CommentsLife Care Medical Devices Ltd today announced the issuance in August 2012 of CE mark for its Keyhole Cup Laparoscopic Access Device. Keyhole Cup addresses a critical need in the laparoscopic surgery market and was developed to advance the standard of care for laparoscopic access.
Vascular Solutions can't dodge illegal marketing lawsuit
April 24, 2013 3:11 pm | by Mass Device | CommentsMinnesota medical device maker Vascular Solutions (NSDQ:VASC) wasn't able to dodge a federal off-label marketing lawsuit over its Vari-Lase varicose vein treatment devices, the company revealed in its latest financial report. A Texas court ruled last month against Vascular Solutions' motion to dismiss a U.S. Attorney's Office complaint...
UIC Building $3.4M Bioscience Research Facility
April 24, 2013 2:50 pm | by The Associated Press | CommentsOfficials have announced a new $3.4 million bioscience research facility at the University of Illinois at Chicago. The 12,000-square-foot facility is being built with state capital funds and money from UIC. Gov. Pat Quinn and UIC officials announced the facility on Wednesday at the proposed site.
FDA's next-gen medtech surveillance bets heavily on unique device identifiers
April 24, 2013 1:47 pm | by Mass Device | CommentsThe FDA laid out plans to revamp its postmarket surveillance of medical devices, and a large part of that has to do with finalizing and implementing a long-awaited Unique Device Identifier program to better track and monitor devices. The federal watchdog agency aims this year to finalize a UDI rule...
Medical device tax: Sen. Max Baucus's retirement and its effect on repeal
April 24, 2013 12:57 pm | by Mass Device | CommentsIt's unlikely that his waning days as chairman of the Senate Finance Committee will see Sen. Max Baucus (D-Mont.) having a "Come-to-Jesus" moment on the medical device tax, but his retirement does change the game on repealing the levy.
