Ablation Therapy System

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*
Comments
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

Resources

July 4, 2022

What does it mean for the FDA to classify a medical device?

One of the most frequent questions we get at Sterling is, “what does it mean for the U.S. Food and Drug Administration (FDA) to classify a medical device?” especially when it comes to...

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....