Carrie Hetrick



Author: Sterling Medical Devices | July 4, 2022

Carrie Hetrick

Resource Director of Regulatory and Clinical Affairs Carrie Hetrick has over 20 years of experience in the medical device industry. Ms. Hetrick leads regulatory, clinical, and quality programs at...
Read More >

Author: Sterling Medical Devices | July 4, 2022

Chris Bradley

Engineering Resource Manager Chris Bradley has been part of the Sterling team for over 14 years. Mr. Bradley has comprehensive experience in software and electrical system design, development,...
Read More >

Author: Sterling Medical Devices | July 4, 2022

Jamme Tan

Resource Director Jamme Tan has been a part of Sterling Medical Devices’ team for over 17 years, serving in multiple roles and advancing in company leadership. Mr. Tan has considerable experience...
Read More >

Author: Sterling Medical Devices | July 4, 2022

Jeff Triolo

Mechanical Resource Manager Jeffrey Triolo has considerable knowledge of all facets of mechanical design and development and manufacturing quality both as a project manager and engineer. His...
Read More >

Author: Sterling Medical Devices | July 4, 2022

Larry Bischoff

Mr. Bischoff brings two decades of product development experience, in both product management and engineering roles to the team of medical device makers at Sterling Medical. Working in both the...
Read More >

Author: Sterling Medical Devices | July 4, 2022

Nick Oshman

Resource Director Nick Oshman has been with Sterling for over 17 years, bringing his quality assurance and management expertise to his role in leading Sterling’s system engineers to help clients...
Read More >

Resources

April 8, 2021

What’s the Difference Between a Class I and Class II Medical Device?

One of the most common questions when it comes to medical device regulation is, “What is the difference between a class I and class II medical device?” Today, we will explore the topic in more...
Read More >
View More Blogs

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.
Read More >
View More Videos

July 12, 2022

Scalp Cooling System

Overview Paxman has been pioneering scalp cooling technology for over a quarter of a century. Paxman’s clinically proven cold cap technology has helped over 100,000 cancer patients in more than 60...
Read More >
View More Case Studies

Need help with your medical device?

Let Sterling Medical Devices show how to bring your idea from concept to prototype to
FDA/CE approval with a free custom project analysis.
Request Free Analysis