Medical Devices News and Research

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LiveData OR-Dashboard completes 2010 IHE North American Connectathon

LiveData, a leading innovator in real-time data integration and display, today announced that the technology underlying LiveData OR-Dashboard, has successfully completed the 2010 IHE North American Connectathon, a proving ground for medical device integration.

30 Jan 2010

Cerner to provide AORN SYNTEGRITY SPF for streamlining EHR perioperative documentation

Helping to streamline electronic documentation processes for perioperative care, CSC and the Association of periOperative Registered Nurses (AORN) announced today that Cerner, a global supplier of healthcare solutions, will be the first to provide AORN SYNTEGRITY™ Standardized Perioperative Framework (SPF) within a surgery and anesthesia management clinical information system. With AORN SYNTEGRITYTM, the amount of clinical staff time needed to configure and support electronic health record (EHR) perioperative documentation can be reduced by as much as 80 percent.

30 Jan 2010

Pioneer Surgical Technology plans to open new office facility in Austin, Texas

Pioneer Surgical Technology, Inc., a leader in innovative medical devices, announced today the company's plan to open a new office facility in Austin, Texas, April 1, 2010. The new facility provides Pioneer greater recruiting access to industry professionals who will help further the growth and development of Pioneer's Spine Division.

30 Jan 2010

NuVasive reports preliminary unaudited financial results for full year ended December 31, 2009

NuVasive, Inc., a medical device company focused on developing products for minimally disruptive surgical treatments for the spine, today announced preliminary unaudited financial results for the full year ended December 31, 2009.

30 Jan 2010

Derma Sciences implements reverse stock split for trading on NASDAQ Stock Market

Derma Sciences, Inc., a specialty medical device/pharmaceutical company focused on advanced wound care, today announced that it would implement an 8-for-1 reverse split of its issued and outstanding common shares, effective for shareholders of record on February 1, 2010, and a proportional reduction of its authorized common and preferred shares.

29 Jan 2010

Contact Solutions' multi-channel solution may help contact centers to improve service and save money

As healthcare companies prepare for a projected increase in contact center traffic, regardless of the outcome of the Obama Administration's healthcare proposals, business leaders are scrambling to ensure they are prepared.

29 Jan 2010

Novella Clinical and OSI Pharmaceuticals expand existing clinical service agreement

Novella Clinical Inc. (formerly PharmaLinkFHI) and OSI Pharmaceuticals, Inc. announced today that the Companies will expand their existing clinical service agreement. Under the terms of the new agreement, effective February 1, 2010, Novella will provide clinical research and related services to OSI for a period of two years as OSI transitions its clinical operations to its new Ardsley, New York campus. Novella will assume use of some of OSI’s facilities in Boulder and employ members of OSI’s Boulder staff.

28 Jan 2010

EnteroMedics to submit an IDE application for next-generation Maestro RC System

EnteroMedics Inc., the developer of medical devices using neuroblocking technology to treat obesity and other gastrointestinal disorders, announced today that, following a recent meeting with the U.S. Food and Drug Administration (FDA) to discuss the Company’s EMPOWER™ study results and the regulatory process, the Company intends to submit an Investigational Device Exemption (IDE) application for a clinical trial to support a possible Premarket Approval (PMA) application for the next-generation Maestro® RC System in the treatment of morbid obesity.

28 Jan 2010

ZOLL Medical's LifeVest Wearable Defibrillator named one of top five innovative medical devices of 2009

ZOLL Medical Corporation, a manufacturer of medical devices and related software solutions, announced today that the Medical Device Network has named the LifeVest® Wearable Defibrillator as one of the five most innovative and life-changing medical devices of 2009.

28 Jan 2010

Encision reports financial results for third-quarter of fiscal year 2010

Encision Inc., a medical device company owning patented surgical technology that is emerging as a standard of care in minimally-invasive surgery, reported its financial results for its third quarter of fiscal year 2010.

28 Jan 2010

Over 8% of medical devices in circulation are counterfeit: WHO

Counterfeit medical products are becoming an international epidemic. According to the World Health Organization (WHO), more than 8% of the medical devices in circulation are counterfeit. The offending products may be assembled from inferior quality components, or worse yet, from fake parts that could contain toxic materials. In either case the dangers are the same. Counterfeit medical devices pose a significant liability to the manufacturers and a health risk to both the patients and healthcare providers that could result in injury, permanent disability, or even death.

28 Jan 2010

Neomend completes $30M Series D funding round

Neomend, Inc., an innovator in sealant and adhesion-prevention products for the surgical marketplace, announced today it has completed a funding round of $30 million, with Clarus Ventures, LLC investing $17 million.

28 Jan 2010

Electrode devices emerge as potential stimulation treatments for depression

Approximately ten to thirty percent of patients with depression do not respond to drug treatments commonly used for the disorder, and this has spurred a search for alternatives. According to Kalorama Information's report "Electrical and Magnetic Neurostimulation," electrode devices that stimulate nerves have emerged as a solution and there is competition among notable device companies to provide the most effective stimulator.

28 Jan 2010

Power-generating rubber films could harness natural body movements

Power-generating rubber films developed by Princeton University engineers could harness natural body movements such as breathing and walking to power pacemakers, mobile phones and other electronic devices.

28 Jan 2010

Access Scientific's PICC WAND receives FDA clearance

Access Scientific has received FDA clearance for The PICC WANDTM, which enables clinicians to insert a peelable sheath for PICC or Midline catheter placement using the new Accelerated Seldinger Technique (AST). The PICC WAND is an all-in-one safety introducer that addresses the over-wire vascular access market, valued at more than $1 billion, by providing faster, safer and simpler vascular access.

27 Jan 2010

Usage of shape memory alloys for fabricating medical devices: Acacia Research subsidiary acquires patent

Acacia Research Corporation announced today that a subsidiary has acquired patents for medical devices using shape memory alloys.

27 Jan 2010

New contract gives U.S. Naval hospitals access to ECRI Institute's medical equipment advisory service and product safety alerts

ECRI Institute®(www.ecri.org), an independent nonprofit that researches the best approaches to improving patient care, announces a new contract, awarded by the U.S. Navy to ECRI Institute, to offer its comprehensive advisory service for managing medical equipment procurement, maintenance, and safety to all U.S. Naval hospitals and medical centers worldwide.

27 Jan 2010

Suneva Medical to present interim data from its Artefill study for NLF correction at the Maui Derm 2010

Suneva Medical, a privately-held aesthetic medical device company, today announced 18-month interim results from its prospective, open-label, five-year safety and patient satisfaction study on Artefill for nasolabial fold (NLF) correction. The study assessed adverse events with Artefill starting at 6-months post treatment. Initial results show the incidence of adverse events with Artefill compare favorably to the current label, and that the majority of patients (88%) reported a high satisfaction rating. Upon completion, this will be the largest and longest duration prospective U.S. clinical study of any dermal filler.

27 Jan 2010

Medtronic' Melody Transcatheter Pulmonary Valve receives FDA approval under HDE

In a significant development for congenital heart disease patients, Medtronic, Inc. (NYSE: MDT), announced today that its Melody® Transcatheter Pulmonary Valve has received U.S. Food and Drug Administration (FDA) approval under a Humanitarian Device Exemption (HDE).

27 Jan 2010

FDA approves first heart valve conduit that can delay need for open-heart surgery

The U.S. Food and Drug Administration today approved the Medtronic Melody Transcatheter Pulmonary Valve and Ensemble Delivery System, the first heart valve to be implanted through a catheter, or tube, in a leg vein and guided up to the heart. This new approach to the treatment of adults and children with previously implanted, poorly functioning pulmonary valve conduits can delay the need for open-heart surgery.

27 Jan 2010

Medical Devices News and Research

LiveData OR-Dashboard completes 2010 IHE North American Connectathon

Cerner to provide AORN SYNTEGRITY SPF for streamlining EHR perioperative documentation

Pioneer Surgical Technology plans to open new office facility in Austin, Texas

NuVasive reports preliminary unaudited financial results for full year ended December 31, 2009

Derma Sciences implements reverse stock split for trading on NASDAQ Stock Market

Contact Solutions' multi-channel solution may help contact centers to improve service and save money

Novella Clinical and OSI Pharmaceuticals expand existing clinical service agreement

EnteroMedics to submit an IDE application for next-generation Maestro RC System

ZOLL Medical's LifeVest Wearable Defibrillator named one of top five innovative medical devices of 2009

Encision reports financial results for third-quarter of fiscal year 2010

Over 8% of medical devices in circulation are counterfeit: WHO

Neomend completes $30M Series D funding round

Electrode devices emerge as potential stimulation treatments for depression

Power-generating rubber films could harness natural body movements

Access Scientific's PICC WAND receives FDA clearance

Usage of shape memory alloys for fabricating medical devices: Acacia Research subsidiary acquires patent

New contract gives U.S. Naval hospitals access to ECRI Institute's medical equipment advisory service and product safety alerts

Suneva Medical to present interim data from its Artefill study for NLF correction at the Maui Derm 2010

Medtronic' Melody Transcatheter Pulmonary Valve receives FDA approval under HDE

FDA approves first heart valve conduit that can delay need for open-heart surgery

Industry Focus - Medical Device eBook

Evaluating new approaches for rare disease genomics

Expanding access to NMR with the Fourier 80 Duo

Advancing Intracellular Delivery with LumiPore®

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