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Sanofi chooses OnPoint clinical trial management system from BioClinica

BioClinica, Inc., a global provider of clinical trial management services, announced today that Sanofi, one of the world's largest pharmaceutical companies, has selected BioClinica's OnPoint as the company's standard CTMS (Clinical Trial Management System).

From Clario 24 Sep 2012

FDA clears Smiths Medical's safety system for epidural anaesthesia injection

Smiths Medical, a leading global medical device manufacturer, today announced that its Portex CorrectInject Safety System for administering neuraxial (spinal and epidural) medication received 510(k) clearance from the U.S. Food and Drug Administration (FDA).

21 Sep 2012

State roundup: HCA fined for kickbacks; Minn. rural health care investigation

The Hospital Corporation of America will pay $16.5 million to settle claims that its subsidiaries had paid a diagnostics firm for referrals, violating federal anti-kickback rules, the Justice Department announced Wednesday. HCA subsidiary Parkridge Medical Center and HCA Physician Services, both provided "financial benefits" to a physician group, Diagnostic Associates of Chattanooga, for referrals to the HCA facilities.

21 Sep 2012

St. Jude Medical’s Eon family of neurostimulators receives European CE Mark approval

St. Jude Medical, Inc., a global medical device company, today announced it has received European CE Mark approval of its Eon family of neurostimulators for patients with intractable chronic migraine. Unveiled at the European Headache and Migraine Trust International Congress in London, this approval includes the Eon Mini neurostimulator, which is the world's smallest rechargeable neurostimulator with the longest-lasting battery in its class, and the Eon and EonC neurostimulators.

21 Sep 2012

Titan Spine receives U.S. patent for competitive interbody devices

Titan Spine, a medical device surface technology company focused on the development of innovative spinal interbody fusion implants, announced today that it has been awarded patent #US 8,262,737 B2 by the United States Patent Office that protects the Company against competitive interbody devices with a roughened surface topography, anti-expulsion edges, and access to a hollow center.

21 Sep 2012

Bionic legs: an interview with Rob Cripe, SVP of Marketing from Tibion

The Bionic Leg is a wearable robotic trainer that is used on mobility impaired patients who need to relearn how to use their affected limb. It is used by clinicians as a tool that is designed to help strengthen stance, improve gait and enhance active motor learning.

19 Sep 2012

Devon Medical Products receives PDAC approval for extriCARE 2400 system

Devon Medical Products, a global medical device manufacturer and distributor, today announced it has received approval from the Pricing, Data Analysis, and Coding (PDAC) contractor for its extriCARE 2400 Negative Pressure Wound Therapy (NPWT) pump and associated bandages and disposable canister.

19 Sep 2012

FDA clears Aptus’ HeliFX Aortic Securement System

Aptus Endosystems, Inc., a medical device company developing advanced technology for endovascular aneurysm repair (EVAR), announced today that it received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its thoracic-length HeliFX Aortic Securement System.

From Medtronic 19 Sep 2012

Biocompatibles, Philips to develop new treatment protocol for trans-arterial embolization

Royal Philips Electronics and Biocompatibles, a BTG international group company, announced a collaboration to advance the use of image guidance to control the delivery of beads during the arterial embolization of hypervascularized tumors today at the annual CIRSE (Cardiovascular and Interventional Radiological Society of Europe) meeting.

15 Sep 2012

Popular Science magazine names UCLA professor among ‘Brilliant 10’

Popular Science magazine has named Aydogan Ozcan, an associate professor of electrical engineering and bioengineering at UCLA, one of the world's "Brilliant 10" scientists in its October 2012 issue.

15 Sep 2012

Supplies and devices may contribute to increase in average cost per patient discharge

Inpatient hospital treatment accounts for the largest proportion of health care spending in the U.S., with the use of diagnostic imaging services such as MRIs, frequently implicated as the probable cause. A new analysis finds that the biggest expense may not be imaging technology but from supplies including medical devices, such as stents and artificial joints.

15 Sep 2012

Trigeminal Nerve Stimulation: an interview with Dr Leon Ekchian, President and CEO of NeuroSigma

Trigeminal Nerve Stimulation (TNS) is a novel medical treatment in which mild electrical signals stimulate branches of the trigeminal nerve in order to change the activity of targeted brain regions. The trigeminal nerve is the largest cranial nerve, and provides sensation to the face and head. Because it is a large sensory nerve, the trigeminal offers a high-bandwidth pathway for electrical signals to enter the brain. The brain areas targeted by TNS are known to play key roles in seizures, mood, and attention.

14 Sep 2012

Viewpoints: Medicaid's role in lowering uninsured rate; Need to protect physicians 'compelled by conscience' to provide abortions

The number of Americans who lack health insurance declined last year, the first drop since 2007. This is, in large part, the result of the health care reform law and better coverage under public programs like Medicaid. This also shows why repealing the health care law or revamping and shrinking Medicaid, as many Republicans want to do, would be disastrous moves.

14 Sep 2012

Acacia subsidiary obtains patent for stent graft technology

Acacia Research Corp announced today that a subsidiary has acquired a patent for stent graft technology.

11 Sep 2012

Bio DG’s novel metal system receives U.S. patent for use in implantable medical devices

Bio DG announced today that its patent for a novel metal system for use as biodegradable material in developing implantable medical devices was granted by the U.S. Patent Office on August 21, 2012.

11 Sep 2012

FDA warns dietary supplement firms in Colorado and Texas

The U.S. Food and Drug Administration today issued warning letters to PruTect Rx, of Highlands Ranch, Colo., and Trinity Sports Group Inc., of Plano, Texas, for promoting products labeled as dietary supplements with claims to treat concussions and prevent or treat post-concussion syndrome and other neurological disorders.

7 Sep 2012

Bionic leg activated by patient’s intent to move introduced by Tibion

Patients who can't use their legs from the effects of multiple sclerosis, stroke, traumatic brain injury, partial spinal cord injury and other debilitating conditions have been given a new 'leg up' with the introduction of the only wearable, lower limb, robotic trainer activated by the patient's intent to move - the Tibion Bionic Leg.

7 Sep 2012

Johnson & Johnson Vision Care develops new educational resource

Soft contact lenses are worn safely and comfortably by millions of people worldwide, and have a long history of providing wearers with a safe and effective form of vision correction when properly worn and cared for. However, research shows that many contact lens wearers are significantly non-compliant in virtually all active steps involved in soft contact lens wear, including hand washing, case hygiene, lens disinfection, and following the recommended lens replacement schedule.

6 Sep 2012

European regulators approve Surefire Infusion System for chemo- and radioembolization procedures

European regulators have approved Surefire Medical's Surefire Infusion System, a next generation device for chemo- and radioembolization procedures. The Colorado-based medical device company today announced that it is launching this product in the European market immediately.

5 Sep 2012

NeuroSigma's external Trigeminal Nerve Stimulation system awarded CE Certification

NeuroSigma, Inc., a Los Angeles-based medical device company, announced today that it received CE Certification for its external Trigeminal Nerve Stimulation (eTNS) system, called the Monarch, for the adjunctive treatment of epilepsy and major depressive disorder, for adults and children 9 years and older.

5 Sep 2012

Medical Devices News and Research

Sanofi chooses OnPoint clinical trial management system from BioClinica

FDA clears Smiths Medical's safety system for epidural anaesthesia injection

State roundup: HCA fined for kickbacks; Minn. rural health care investigation

St. Jude Medical’s Eon family of neurostimulators receives European CE Mark approval

Titan Spine receives U.S. patent for competitive interbody devices

Bionic legs: an interview with Rob Cripe, SVP of Marketing from Tibion

Devon Medical Products receives PDAC approval for extriCARE 2400 system

FDA clears Aptus’ HeliFX Aortic Securement System

Biocompatibles, Philips to develop new treatment protocol for trans-arterial embolization

Popular Science magazine names UCLA professor among ‘Brilliant 10’

Supplies and devices may contribute to increase in average cost per patient discharge

Trigeminal Nerve Stimulation: an interview with Dr Leon Ekchian, President and CEO of NeuroSigma

Viewpoints: Medicaid's role in lowering uninsured rate; Need to protect physicians 'compelled by conscience' to provide abortions

Acacia subsidiary obtains patent for stent graft technology

Bio DG’s novel metal system receives U.S. patent for use in implantable medical devices

FDA warns dietary supplement firms in Colorado and Texas

Bionic leg activated by patient’s intent to move introduced by Tibion

Johnson & Johnson Vision Care develops new educational resource

European regulators approve Surefire Infusion System for chemo- and radioembolization procedures

NeuroSigma's external Trigeminal Nerve Stimulation system awarded CE Certification

Industry Focus eBook - Medical Devices (3rd Edition) eBook

Designing fluidic architecture for scalable diagnostic platforms

Evaluating new approaches for rare disease genomics

Expanding access to NMR with the Fourier 80 Duo

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