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Wherever you are in your product development lifecycle,
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Medical Device Conference, Tradeshows & Events

Explore our list of upcoming medical device conferences, trade shows and events! Whether it is a medical device conference or medical trade show, we aim to meet fellow experts in the medical device industry and share our expertise with fellow attendees. We hope to see you at one of these upcoming events.

RESI NYC 2017

New York Marriott Marquis, 1535 Broadway, New York, NY 10036

MD&M West

Anaheim Convention Center, Anaheim, CA

MD&M East 2019

655 W 34th St, New York, NY 10001 (Jacob K. Javits Convention Center)

COVID-19 Regulatory Assistance for Medical Device EUAs

Online - Webinar

Are you struggling to achieve regulatory approval for a potentially life-saving medical device in this current COVID-19 environment? You may be able to file for an Emergency Use Authorization and receive regulatory approval through an expedited process. This will get your product to market much faster. In our webinar, COVID-19 Regulatory Assistance for Medical Device […]

BIOMEDevice Virtual Conference

Are you interested in learning about the latest changes in medical device design, robotics development, and digital health? Join us at the BIOMEDevice Virtual Conference! April 6-7, 2021 This unique event will feature tech talks, panel discussions, and keynote speakers discussing: Research and Development Product Development 3D Printing & Smart Manufacturing Digital Health: Design & […]

BIOMEDevice Boston

Want to learn about the latest technologies and products in the industry, listen to expert-led discussions and presentations and network with industry professionals? Join us at BIOMEDevice Boston on September 21-22, 2021 at the Boston Convention Center! The in-person event is designed for C-suite professionals and engineers in the medical device industry who are looking […]

Artificial Intelligence and Machine Learning: Making Medical Devices Smarter

Are you interested in learning more about improving medical devices with artificial intelligence and machine learning without compromising safety? These technologies are enabling medical devices to provide clinicians tools for earlier disease detection, more accurate diagnosis, and development of personalized diagnostics and therapeutics. However, along with these added capabilities, the U.S. Food and Drug Administration […]

Global MedTech Regulatory Trends: True Quality Summit Series

Watch Live: August 30-September 1 Then available on-demand MedTech regulations are evolving. Increasing globally, changing constantly, creating headaches for you and medical device companies around the world. It's your responsibility to assess the changes unfolding to fully understand the impact on your business and product. Are you ready to adapt? To help you navigate the […]

RAPS Convergence 2022

Are you looking to connect with your peers in regulated industries, health authorities, and notified bodies across the healthcare products industry and learn about emerging innovations and best practices across the healthcare products sector? Join us at the RAPS Convergence 2022 Conference in Phoenix, AZ, September 11-13. This in-person event is a great opportunity for […]

Resources

February 18, 2021

The New EU Medical Device Software Requirements

With the EU’s new medical device software (MDSW) requirements, the guidance related to qualification, classification, clinical evaluation and cybersecurity present challenges for software as a...
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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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