GUILFORD, Conn.--(BUSINESS WIRE)--Defibtech, LLC, a designer and manufacturer of automated external defibrillators (AEDs) and other resuscitation equipment, announced today that it has signed an ...

This story was originally published on MedTech Dive. To receive daily news and insights, subscribe to our free daily MedTech Dive newsletter. Defibtech has recalled a chest compression device after ...

GUILFORD, Conn.--(BUSINESS WIRE)--Defibtech, LLC, a Nihon Kohden company based in Guilford, Conn., announced today that its board of directors has unanimously chosen Robert Reinhardt as Defibtech’s ...

Lincoln International, a leading global mid-market investment bank, has announced that Defibtech, LLC (“Defibtech”) has been sold to Nihon Kohden Corporation (“Nihon Kohden”), a publicly traded ...

Defibtech and Master Medical Equipment partner on Leasing Program to Expand Access to Lifesaving Technology GUILFORD, Conn. – Defibtech, a leading manufacturer of lifesaving medical equipment, today ...

The Guilford, Conn.-based manufacturer of AEDs and other resuscitation equipment will continue to operate independently as a wholly owned subsidiary of Delaware-based Resuscitation Solution Inc., a ...

Defibtech introduces the newest generation Automatic External Defibrillator (AED). Now there is something you can do to improve the odds dramatically with a solution that is both easy to use and ...

January 13, 2025, Guilford, CT – Defibtech, a U.S. manufacturer of life-saving medical equipment, welcomed Senator Richard Blumenthal to their Branford, CT manufacturing facility on Friday to ...

Defibtech, a U.S. manufacturer of life-saving medical equipment, announced today the release of an expansion to their Lifeline VIEW and Lifeline ECG product lines in the United States. The new ...

GUILFORD -- A building sits at 741 Boston Post Road that houses a company that exports equipment that may help save a life. Defibtech has received recognition from ThinkGlobal Inc. as "Exporter of the ...

The class I recall announced by the Food and Drug Administration is a worldwide voluntary recall of Lifeline AED and ReviveR AED units shipped with 2.004 software or earlier. May 03, 2011 Owners of at ...