Kelly W. Elliott, RN MS
Founder, President, & CEO
MS. ELLIOTT FOUNDED CUBE MEDICAL INNOVATIONS, INC. WITH TWO GOALS IN MIND:
- Assist medical device inventors in the design, development, and commercialization of their idea and
- Bring new disruptive technologies to clinicians to change and improve the standard of care.
As a registered nurse in the medical-surgical and open-heart ICUs, cardiac catheterization lab, Ms. Elliott’s strong clinical background has enabled Ms. Elliott to design and conduct clinical trials in a large variety of applications. Ms. Elliott has held executive-level positions at multiple medical device companies, successfully designing and executing clinical regulatory strategies and clinical trials resulting in new medical device approvals, new medical indications, and dozens of publications in peer-reviewed medical journals. Through the founding of Cube Medical Innovations, Inc., Ms. Elliott is able to assist physicians and other medical device inventors in conceptualizing, creating, and commercializing their idea.
Chuck Walker
SVP Operations
Chuck Walker is Senior Vice President of Operations for Cube Medical Innovations, Inc.
Before joining Cube, Chuck spent 30 years in Silicon Valley’s electronics manufacturing industry living and working in the SF Bay Area. Chuck’s background is in business development, program management, and product development, primarily serving the medical device, space, defense, and commercial industries. He has overseen and managed numerous cross-functional, customer focus teams involved in product development and bringing those products to market.
In April of 2018, Chuck joined the Cube Team and moved his family to Colorado Springs, Colorado in October of 2018. He now lives and works in the Colorado Springs area living with his wife and son.
Chuck works closely with Cube’s sister company, Eminence Clinical Research, Inc. serving as Vice President of Business Development. Eminence Clinical Research, Inc. is a clinical research organization specializing in providing the infrastructure to medical device startups and small businesses requiring 510(k), QMS, and regulatory compliance.
Thomas Shilling
Sr. Director of Program Management
With a 25 year background of global regulatory affairs, business management systems and new product development, Thomas is more than well-equipped to lead new product concepts to success.
After receiving an MBA, as well as certification as an ISO lead Assessor from the Governing Board of the International Register of Certificated Auditors, he has served companies, large and small, in obtaining certifications for ISO 13485 Quality Management Systems (FDA-QSR), as well as clearances for marketing globally. These include the CE Mark as well as 510(k) clearances from the FDA for medical devices.
His talents are recognized for mapping of the business and regulatory path to success in medical device development, from concept through
actualization. Each map is custom developed for each Cube client. You are then monitored, guided, and supported along your program by the Cube team.
The decision to utilize his talents provides for a clear identification of the elements of your program forward thus enabling more accurate budgeting, determination of timelines and certainty of success.
Note: The full resume of Thomas Shilling, MBA is available upon request.