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September 28, 2012
CEO says the acquisition is part of Medtronic's goal of globalization.
The device is the next-generation version of Clearbridge's ClearCell System.
September 24, 2012
The agency's OK comes following a warning letter earlier in the year.
The newly created position is meant to drive the development of Utah's life sciences sector.
The new location will provide a nexus for China and other regional clients.
September 21, 2012
The medical device giant is adding BridgePoint to its Interventional Cardiology Division.
The two companies are focused on the treatment of epilepsy.
Device now can be used in patients 65 and older.
The new hire will focus heavily on R&D for pharmaceutical and medical device customers.
September 20, 2012
The trade fairs in Germany provide a forum for players from all corners of the medical technology industry to come together.
September 19, 2012
The needles are targeted toward diabetes patients who fear needles due to pain or discomfort.
The system is geared toward women with dense breast tissue.
The company manufactures podiatric devices.
September 18, 2012
The devices are available in both the U.S. and the E.U.
Iris will join Danaher's Beckman Coulter diagnostics business.
September 17, 2012
Latest delay could cost the company NYSE listing.
Officials claim the space of interoperability needs to be developed.
September 14, 2012
The New Hampshire facility is hoped to provide 25 new jobs.
Rep. Paulsen and industry advocates believe government is unprepared for the implementation of the tax.
September 13, 2012
The facility is the company’s first in Latin America.
September 12, 2012
The system is relatively affordable, a big attraction for emerging markets.
New hire brings experience in product innovation.
Citing the medical device excise tax, the company looks outside the United States for new business opportunities.
September 11, 2012
Research company details how the market share is divided globally.
The new version of the Impella is doubly powerful, company claims.
Entries may still be submitted until the end of October.
September 10, 2012
Researchers believe Intact Vascular’s new technology will not best existing technology.
The CE Mark approves the system to treat chronic pain and patients who need MRIs.
This report is part of a slew of steps the FDA is taking to keep the promises of MDUFA.
September 7, 2012
The device is being updated, and the new version will be re-submitted for approval.
September 6, 2012
The device received European approval earlier this year.
Restore Medical Solutions was one of the first companies to participate in the accelerated device development program.
September 5, 2012
The cover is intended specifically for obese patients.
The news comes soon after the release of a new Arrow catheter earlier this month.
The company received the CE Mark a year after it received FDA clearance.
The investment will go toward the development of a blood flow monitoring device.
Specialty Manufacturing’s expansion more than doubles its plant size.
The new Canton location will manufacture polymer tubing.
The two companies will join forces on a self-injection drug delivery system.
September 4, 2012
The company hopes to be one of the few welding companies to achieve the medical device ISO standard.
