What We Believe
Mainstream stands for integrity – of our people, our products, and our partners. We will enable our customers to improve patient outcomes by providing innovative medical instruments, improved accessories, and exceptional services enhanced for the overall safety and effectivity of the medical marketplace.
Quality Standards
The products and services offered in the Mainstream family provide state of the art medical technology. We aim to raise the medical industry’s standard of safety and quality with our innovative packaging solutions, manufacturing solutions, and OEM products, thus improving the quality of life for the patients we ultimately serve.
We Are Committed To...
Dana Wilcox
Chief Executive Officer
Dana joined Mainstream Medical Devices in April 2019, bringing over 25 years of experience to help drive the company’s growth. She identified the need for a “right-sized” supplier in the sterile packaging industry, complementing Mainstream’s focus on single-use, disposable instruments. Dana has 30+ years of experience, most recently as Director of Operations at OriGen Biomedical. Before OriGen, she gained valuable management and engineering experience in her roles at Luminex Corporation and Abbott. Dana holds a Bachelor of Science in Mechanical Engineering with a Biomedical Specialization from Southern Methodist University and a Master of Science in Science and Technology Commercialization from the University of Texas at Austin.
Aaron Bailey
President
Aaron has 30+ years of experience researching, developing, and commercializing medical devices. “Leading cross-functional corporate teams and their surgeon counterparts has been my privilege and my passion,” Aaron says. His experience at small, medium, and large companies provides a unique perspective on the industry. Aaron has a proven track record collaborating with the best talent globally, organizing franchise strategies, and commercializing state-of-the-art medical products. Aaron earned a Bachelor of Science in Mechanical Engineering from Texas A&M University and a Master of Science in Bio-Mechanical Engineering from the University of Texas at Austin.
Casey Atkins
Director of Packaging
Casey has 11+ years of experience in the medical device industry. She has worked in management roles in both Operations and Technology Transfer, that include companies such as Smith + Nephew, Integra LifeSciences. Her experience in both device manufacturing and product development in technology transfer roles has given her a unique set of skills. She has a history of creating systems and process improvements that drive operational efficiency while maintaining high quality standards. She received a Bachelor of Exercise and Sports Science Degree from Texas State University and is also an ASQ certified Quality Auditor.
Ken Thoma
Director of Quality
Ken has 30+ years of experience in the medical device industry that includes orthopedics, active implantables, and in-vitro diagnostics. He has worked in management roles in both Operations and Quality, that include companies such as Smith + Nephew, Integra LifeSciences, and Cyberonics Inc. This experience has given him insight into the challenges that are encountered from design transfer to post-market activities. Ken has stated that “At Mainstream Medical Devices, it is essential for our clients and customers to know that we are looking out for them in order to meet their vision and goals in a compliant and
efficient way.”