Category: AppleSyndicate content

Breast cancer: Faulty breast implants in France | On Call

December 21, 2011 by MassDevice staff

French authorities may ask 30,000 women to have a potentially defective type of breast implant removed.

MassDevice On Call

MASSDEVICE ON CALL — French authorities need to decide whether or not they're going to ask 30,000 women to have their breast implants removed.

The potentially defective implants were supplied by Poly Implant Prothese and contain a non-authorized silicone gel that causes high rupture rates.

"We have to remove all these implants," Dr. Laurent Lantieri, a plastic surgeon on a special committee investigating the issue told the Liberation newspaper. "We're facing a health crisis, linked to a fraud."

Diabetes: WPI team gets $1.2M for diabetes care app | Funding Roundup

December 13, 2011 by MassDevice staff

A research team from Worcester Polytechnic Institute lands $1.2 million from the National Science Foundation to develop a diabetes care smart phone app.

A research team from Worcester Polytechnic Institute won a $1.2 million grant from the National Science Foundation to develop a smart phone app for people with advanced diabetes.

The proposed application, currently named "sugar," will link a patient's smart phone, glucose meter and scale to track and archive blood sugar levels and weight. Patients with foot ulcers will be able to use the phone's camera to capture and analyze images of the lesions. +3 | CardioMEMS CEO on FDA ruling, iPhone glucose meter, Stryker cuts 160 jobs

December 9, 2011 by MassDevice staff

The top three medical device stories for December 9, 2011.

Plus 3

Say hello to MassDevice +3, a bite-sized view of the top three med-tech stories of the day. This latest feature of's coverage highlights our three biggest and most influential stories from the day's news to make sure you're up to date on the headlines that continue to shape the medical device industry.

If you read nothing else today, make sure you're still in the know with MassDevice +3.

Diabetes: FDA clears iPhone glucose meter | On Call

December 8, 2011 by MassDevice staff

Sanofi's iBGStar becomes first iPhone glucose meter to land FDA clearance.

MassDevice On Call

MASSDEVICE ON CALL — Sanofi’s (NYSE:SNY) iPhone glucose meter, the iBGStar, landed 510(k) clearance from the FDA, making it the first iPhone glucose meter to win a nod from the federal watchdog agency.

The company's website describes the meter as "is the first available blood glucose meter that seamlessly connects to the Apple iPhone and iPod touch for the flexibility to manage your diabetes whenever, wherever."

Automated defibrillators are a bad choice for hospitals | On Call

November 28, 2011 by MassDevice staff

The new automated defibrillators found in hospitals save less lives than older, low-tech defibrillators.

MassDevice On Call

MASSDEVICE ON CALL — After an American Heart Assn. recommendation in 2000, hospitals around the country spent millions updating to automated defibrillators to improve the chances of saving patients who go into sudden cardiac arrest.

Research shows that the newer defibrillators, now present in almost every hospital in the country, actually save fewer lives than the older, low-tech defibrillators.

Surgical robot brings precision to eye surgery | On Call

November 1, 2011 by MassDevice staff

PhD student Thijs Meenink unveils his surgical robot for ophthalmological procedures, an untapped market in the U.S.

MassDevice On Call

MASSDEVICE ON CALL — A new surgical robot designed to bring ease and precision to eye surgeries may hit the market, if inventor Thijs Meenink can defend his PhD thesis work on the machine.

Meenink, a student at Eindhoven University of Technology, plans to commercialize the novel robot after he obtains his doctorate.

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House bills target FDA med-tech approval process | On Call

October 27, 2011 by MassDevice staff

House Republicans target the FDA's review and approval process of medical devices with 10 new bills.

MassDevice On Call

MASSDEVICE ON CALL —House Republicans introduced 10 bills aimed at the FDA's medical device review and approval process.

The 10 bills, sent to the Energy & Commerce Committee, detailed proposed measures to reform the predictability, consistency and transparency of the federal watchdog agency's med-tech review process.

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