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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

FDA medical device regulations graphs.

April 4, 2022

FDA Medical Device Regulation Guidance for 2022

In the United States, the U.S. FDA (Food and Drug Administration) provides medical device regulation through the CDRH (Center for Devices and Radiological Health). The agency recently released...
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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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people developing a product

November 23, 2020

Sterling Helps Print Parts Win Contract with City of New York for Production of Medical-Grade Nasal Swabs

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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