Sterling Medical Devices specializes in the design, development, and testing of medical devices. Sterling addresses every aspect of the development process: software, electronics, mechanical, quality, and compliance. Our goal is to make sure you get the FDA approval and CE Marking you need to bring your device to market.

Sterling Medical Devices was founded in 1998 as SterlingTech, Inc. by President and CEO Daniel Sterling. The company’s early years were focused around the development and testing of medical device software. As our clients’ needs and expectations grew, so did Sterling’s services and medical device development capabilities.

Today, with two offices and over 50 employees, Sterling specializes in the complete design, development, and testing of medical devices. Though our services and capabilities have expanded to include system, electronic and mechanical disciplines, Sterling has not forgotten its software roots. Through our “Sterling Approach” software-driven devices controlling hardware and systems are developed in an optimal way which leads to better estimates, fewer hardware iterations, and earlier market release.

Sterling has developed more than 300 medical device products for over 100 companies, ranging from Class II diagnostic and therapeutic systems to Class III implantable devices, using embedded systems, PC based devices, smartphones/tablets, and web/Cloud services. We are proud to have worked with such prestigious organizations as Covidien, St. Jude Medical, Medtronic, Boston Scientific, Johnson & Johnson, and many more. We have also partnered with a number of early-stage companies to help them bring new products to market. In every case, we produce the right product in the right timeframe with the right budget.