Device Reporting News Today

The advent of the COVID-19 rapid antigen test launched at-home diagnostics to the forefront of conversation in the life sciences industry. Many believe this is only the beginning. As...

On February 2, 2024, the U.S. Food and Drug Administration (FDA) published a final rule amending the device good manufacturing practice (GMP) requirements of the Quality System...

The $479 million amount is only a minimum for one of the device industry's most serious recalls, and doesn't cover patient injuries or deaths.

The FDA is clarifying Philips claims that it has shipped 2.46 million replacement respiratory devices and repair kits in the U.S.

Amendments to SEC Paragraphs Pursuant to SEC Staff Accounting Bulletin No. 119 and Update to SEC Section on Effective Date Related to Accounting Standards Update No. 2016-02, Leases , which amended... | March 31, 2023

Dublin, Dec. 30, 2022 (GLOBE NEWSWIRE) -- The "A Comprehensive View of Medical Device Post-Market Regulations and Challenges -Complaint Handling, MDR...

Allow me to set the stage. Our plaintiff claims he felt a nagging pain in his shoulder for months and finally went to see the local orthopedic surgeon. The surgeon apparently informed...

Allow me to set the stage. Our plaintiff claims he felt a nagging pain in his shoulder for months and finally went to see the local orthopedic surgeon. The surgeon apparently informed...

The FDA has received more than 90,000 reports of problems — including 260 mentioning deaths — in Philips' massive respiratory devices recall. 

/PRNewswire/ -- The "Global MedTech Healthcare IT Industry Competitive Landscape" report has been added to ResearchAndMarkets.coms offering. This report...