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Medical Device Industry News & Trends



Author: Dan Sterling | September 29, 2009

Sterling Expands Medical Device Development Capabilities, Hires Larry Bischoff

SterlingTech Software Expands Medical Device Development Capabilities, Hires Larry Bischoff as Embedded Systems Manager New hire bolsters firm’s hardware and software development solutions Rochelle...
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Author: Dan Sterling | February 10, 2009

Sterling Receives ISO 13485 Certification For Medical Devices

SterlingTech Software, a leader in custom software solutions for the medical device industry, announced today that it has received ISO 13485 Certification. ISO 13485 is an internationally recognized...
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Author: Dan Sterling | December 4, 2007

Sterling Receives State of New Jersey Grant for ISO 9001 Certification

John Campbell, Veteran Director of Quality Assurance, to spearhead project SterlingTech Software, a leader in custom software solutions for the medical device industry, announced today that it has...
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Author: Dan Sterling | April 17, 2007

Sterling Expands its Operations into New Facility

SterlingTech Software, a leader in custom software solutions for the medical device industry, announced today that it has dramatically expanded its operations. SterlingTech has completed the purchase...
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Resources

FDA 510(k)-Clearance-Approval

January 10, 2022

The COVID-19 Pandemic and 510(k) Clearances

The global COVID-19 pandemic, and the subsequent public health emergency it created, changed much about our everyday lives, and the medical device industry is no exception. To respond quickly to...
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5 Mistakes Medical Device Startups Make

February 18, 2021

5 Mistakes Medical Device Startups Make

Startups are the lifeblood of medical device innovation. Without universities researching ways to solve pressing healthcare problems or doctors with experience in a particular field who have an idea to develop a prototype medical device that could help patients, the future technologies needed to help save lives wouldn't happen. But the long, arduous road through the FDA submission process to get market approval can take a long time and cost a lot of money without help. Sterling Medical Devices has been helping startups through the FDA approval process since 1998 without ever having a submission rejected.
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Breathing-Pacemaker

September 8, 2020

Breathing Pacemaker

Sterling Medical Devices performed design services for a Class III breathing pacemaker with Major Level of Concern software, intended for use by patients who have lost neurological control of respiration. This life-sustaining device is comprised of two main components: an internal passive receiver and an external controller....
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