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Wherever you are in your product development lifecycle,
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Erik Hilliard



Author: General Marketing | July 4, 2022

Erik Hilliard

Erik Hilliard has been with Sterling Medical Devices, now Vantage MedTech for over 18 years. As a versatile leader, Erik brings a wealth of industry experience to his role. He currently serves...
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Author: General Marketing | September 12, 2023

Jay Kendall

Jay has more than 20 years’ experience in the medical device industry, serving as a leader in sales, marketing, and training & education at Zimmer Biomet. Throughout his career, he’s...
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Resources

doctor pointing to screen with icons

April 30, 2020

Device Manufacturers Face Challenges to Balance Opportunity and Risk

With an increased focus on technology advancement and product development, medical device manufacturers are beginning to improve their devices and seize new opportunities. However, this comes with an...
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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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