Jay Kendall

Interested in learning more about how we can work together in your current or next medical device design project?

Just fill out this form and we’ll be in touch!

Name*
First Last
Email*
Phone*
Title
Company*
Message*
Name
This field is for validation purposes and should be left unchanged.

Wherever you are in your product development lifecycle,
Sterling can help.

P: 201-877-5682
F: 201-301-9169
info@sterlingmedicaldevices.com

Jay Kendall

Vice President of Business Development

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 demonstrated an unwavering commitment to meticulous planning and flawless execution, as evidenced by his leadership of the largest commercial product launch in the history of the orthopedic industry. At Vantage MedTech, Jay leads the Business Development efforts of the company with a focus on creating mutually beneficial and long-lasting partnerships with Vantage’s clients. Jay holds a bachelor’s degree in marketing from Kent State University in Kent, OH.

Share this!

Resources

Man conducting third party compliance audit.

February 2, 2023

Uncovering the Benefits of Third-Party Compliance Auditing

The importance of maintaining a high level of quality and compliance can’t be overstated for medical device companies. Failing to do so can put patients at risk, land you in hot water with...

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.

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....

Interested in learning more about how we can work together in your current or next medical device design project?

Just fill out this form and we’ll be in touch!

Jay Kendall

Jay Kendall

Share this!

Resources

Uncovering the Benefits of Third-Party Compliance Auditing

5 Mistakes Medical Device Startups Make

Breathing Pacemaker

Need help with your medical device?