MassDevice Staff

The Massachusetts Medical Devices Journal is the online journal of the medical devices industry in the Commonwealth and New England, providing day-to-day coverage of the devices that save lives, the people behind them, and the burgeoning trends and developments within the industry.

Posts by MassDevice Staff

Devices & Diagnostics

GE Healthcare forms two new partnerships, expands market reach

GE Healthcare signed two new deals that will expand its footprint in the radiotherapy and diagnostics market in China and offer mass spectrometry support in North America. GE signed a memorandum of understanding with Beijing-based Concord Medical Services Holdings Ltd., which operates the largest network of radiotherapy and diagnostic imaging centers in China. They will […]

Devices & Diagnostics

Sen. Scott Brown talks medical device tax repeal at Covidien

Massachusetts Senator and GOP presidential hopeful Scott Brown told Covidien plc (NYSE:COV) employees that the impending medical device tax was “a wet blanket over the industry” when he toured the med-tech giant’s headquarters in Mansfield, Mass., yesterday. An active challenger of the impending medical device tax, Brown’s latest legislation aimed at repealing the bill was […]

Devices & Diagnostics

Unnecessary stents cost Maryland hospital $1.8M in legal settlement

A Maryland hospital paid $1.8 million to settle allegations that senior leadership failed to properly address complaints of unnecessary stenting lodged against former cardiologist Dr. John McLean. McLean was convicted of health care fraud last month over insurance claims he filed on unnecessary stents implanted in Medicare and Medicaid patients. McLean was also charged with […]

Devices & Diagnostics

Covidien announces $2 billion stock repurchase program

Covidien Plc.’s (NYSE:COV) board of directors approved a $2 billion stock repurchase program today. “The board’s approval of this share repurchase program reflects its confidence in the continued growth of Covidien’s business, our sustainable free cash flow and our commitment to enhance shareholder value,” president & CEO José Almeida said in a press release. The […]

Devices & Diagnostics

Insulin pump hacking not a threat, Medtronic says

Medtronic Inc. (NYSE:MDT) isn’t in an uproar over recent reports of a hacked insulin pump that could discretely deliver dangerous doses of insulin to a wearer. “To our knowledge, there has never been a single reported incident outside of controlled laboratory experiments in more than 30 years of device telemetry use, which includes millions of […]

Devices & Diagnostics

Boston Scientific to spend $37 million on Irish R&D facility

Boston Scientific Corp. (NYSE:BSX) plans to spend $37 million on overseas research and development, this time at its R&D facility in Clonmel, Ireland. The Natick, Mass.-based company hopes to jump-start development of a next generation cardiac rhythm management system. The funding is partially supported by a grant from IDA Ireland, a quasi-public investment promotion agency, […]

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Devices & Diagnostics

St. Jude, Illumina buying back shares

St. Jude Medical Inc. (NYSE:STJ) and Illumina Inc. (NSDQ:ILMN) both announced share repurchase programs this week after reporting second quarter earnings. St. Paul, Minn.-based St. Jude’s board of directors authorized up to $500 million to repurchase shares, which will be made available for general corporate purposes and for offsetting dilution associated with employee benefit plans. […]

Devices & Diagnostics

Medtronic taking part in GI Dynamics private placement

Medtronic Inc. (NYSE:MDT) is deepening its commitment to GI Dynamics Inc. by participating in a private placement concurrent with the Lexington, Mass.-based company’s initial public offering in Australia next week. The Minneapolis, Minn.-based medical device giant, which has already invested $15 million in the company, has signaled its intention to be a part of a […]

Devices & Diagnostics

Premarket review standards updated by FDA

The FDA released a notice yesterday announcing updated, withdrawn and modified standards that the agency will use in reviewing premarket applications for a variety of medical devices. The standards can be used to support 510(k) applications by demonstrating “reasonable assurance of safety and/or effectiveness for many applicable aspects of medical devices.” Far from ditching the […]