Medical Devices Expert Witnesses in Tennessee

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Medical Devices expert witnesses practice in a variety of fields, including product design, regulatory compliance, and clinical use. Some of the most common specialties include biomedical engineering, FDA regulatory affairs, human factors, and device failure analysis. They can opine on the effects of design defects, misuse, labeling errors, and adverse events on patient safety and outcomes.

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Average Medical Devices Expert Witnesses Court Fees

Review Fee

Deposition Fee

Court Fee

Medical Devices Experts in Tennessee

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  • Review Fee $400/hr
    Deposition Fee $450/hr

    This expert received a Ph.D. in Biomedical Physics and is board certified in Radiology. She is a certified Radiation Safety Officer and a member of the American College of Medical Physics and American Nuclear Society.

    Medical Physicist, A university-affiliated hospital in NC

    Doctor of Philosophy (PhD), University of California Los Angeles

    Raleigh,

    Tennessee

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  • Review Fee $250/hr
    Deposition Fee $250/hr
    Court Fee $350/hr

    This decorated expert has a quarter century of electrical engineering experience, earning graduate qualifications at MIT, where his work had important biomedical applications. He is a member of several professional societies such as the Institute for Electrical and Electronic Engineers and Virginia Academy of Science. Active in research, he has won numerous grants and has been published widely. He has consulted on IP issues in the past and holds several patents for his inventions.

    Professor of Electrical Engineering, Top Ranking University

    Doctor of Philosophy (PhD), Massachusetts Institute of Technology

    Buena Vista,

    Virginia

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  • Review Fee $350/hr
    Deposition Fee $350/hr
    Court Fee $350/hr

    This medical device sales professional has been in the industry since 1999. He earned his B.A. in Economics from Emory University and eventually went to work for Boston Scientific as a Territory Sales Manager in Men's and Women's Health. After 10 years with Boston Scientific, the expert joined St. Jude Medical's Neuromodulation device team as a Territory Manager in the Gulf Coast region. He was involved in 800+ implants and worked on device servicing for an additional 200+ patients. The expert left St. Jude at the end of 2015 and is now a Business Development and Sales Manger for a different device company in a separate product category.

    Gulf Coast Regional Endourology Specialist, Ostomy / Urology / Wound Care Device Manufacturer

    Bachelor of Arts (BA), Emory University

    Fairhope,

    Alabama

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  • Review Fee $550/hr
    Deposition Fee $600/hr
    Court Fee $600/hr

    This highly credentialed biomedical engineer has significant experience in the design and development of cardiothoracic medical devices. He earned his Master's degree from Georgia Tech and the Emory University School of Medicine; After six years of industry experience he returned to academia and obtained the PhD from the University of Aarhus in Denmark. Then at the Aarhus University Hospital he achieved the Doctor Medicinae (DrMed) degree, which denotes medical research expertise above and beyond a PhD. He is an active member of several scholarly societies in the biomedical field and is a regular reviewer of the Annals of Biomedical Engineering, the Journal of Surgical Research, and Cardiovascular Engineering and Technology. He currently serves on the biomedical engineering faculty of a major Southern university.

    Owner, A Biomedical Consultancy Firm in AR

    Doctor of Philosophy (PhD), University of Aarhus

    Fayetteville,

    Arkansas

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  • Review Fee $250/hr
    Deposition Fee $350/hr
    Court Fee $350/hr

    This highly qualified expert has over a decade's experience in orthopedic trauma medical device sales in both a field capacity as well as executive, following a career in law enforcement in special operations. Extensive experience, has been in thousands of surgical procedures; and has previously conducted hundreds of criminal investigations. At DePuy Synthes, Companies of Johnson & Johnson, he managed a large territory in Orthopedic Trauma devices, providing clinical expertise and training to surgeons and hospitals regarding the proper use of the company's trauma line. He is currently the Vice President at another orthopedics device company specializing in carbon fiber trauma and oncology products. In summary, this expert has sales, compliance and sales training experience, with a Law Enforcement, Collegiate Athletics, and a military academy background.

    US VP, Sales and Strategic Products, A medical device company

    Bachelor of Science (BS), University of Tennessee

    Bridgewater,

    Virginia

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  • This highly qualified expert has extensive experience in the fields of cancer, biomedical research, pre-clinical animal research and ethics, and drug development, among others. After earning his BS from East Carolina University and his MS from The University of North Carolina at Greensboro, this expert completed his PhD in genetics and molecular biology at The University of North Carolina, Chapel Hill. He also went on to complete his MBA in biosciences management at North Carolina State University. This expert is an active member of the American Association of Immunologists, the Society for Leukocyte Biology, and the American Association for Cancer Research. In addition to being extensively published, he is the current associate editor of Frontiers in Immunology and Frontiers in Microbiology. Further, this expert has been engaged in a variety of university program development and research operations leadership roles throughout his career. Among his former roles, he has served as a research analyst with the Center for Human Genetics at Duke University Medical Center, a research associate for microbiology and immunology at The University of North Carolina Chapel Hill, and as an assistant professor of inflammatory diseases at Virginia-Maryland College of Veterinary Medicine. This expert currently maintains two assistant professorships at a public medical school in Virginia, in addition to his primary role as an associate professor of inflammatory diseases at a veterinary medicine education school.

    Associate Professor, A veterinary medicine education school in VA

    Master of Business Administration (MBA), North Carolina State University

    Virginia

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Related Specialties

What Can a Medical Devices Expert Witness Opine On?

Device Design

Creating functional medical device prototypes.

Regulatory Submission

Preparing documents for regulatory approval.

Quality Assurance Testing

Ensuring device safety and efficacy.

Clinical Evaluation

Assessing device performance in clinical settings.

User Training

Educating users on device operation.

Post-Market Surveillance

Monitoring device performance after launch.

FAQs for Medical Devices Expert Witnesses

What is the role of a medical devices expert witness?

A medical devices expert witness is a qualified specialist who explains device design, safety, and standards in legal cases. They assist by reviewing records, testing devices, writing reports, and testifying to clarify complex technical issues.

What types of cases can a medical device expert witness opine on?

A medical device expert witness opines on product defects, FDA compliance, labeling, adverse events, device failures, recalls, design, testing, manufacturing, and post‑market surveillance.

How can a medical devices expert witness strengthen product liability claims?

A medical devices expert witness strengthens product liability claims by explaining device design, testing, standards compliance, and causation in clear, evidence-based testimony.

What qualifications should attorneys prioritize in a medical devices expert witness?

Attorneys should prioritize a medical devices expert witness with advanced clinical or engineering credentials, device-specific experience, regulatory knowledge, and strong testifying history.

How does a medical devices expert witness evaluate device design compliance?

A medical devices expert witness evaluates device design compliance by reviewing design controls, risk management, testing data, regulatory standards, and documentation against FDA and ISO requirements.

What is Expert Institute’s process for selecting medical devices expert witnesses?

Expert Institute delivers a tailored approach to connect you with top-tier experts. We identify actively practicing professionals who meet your exact criteria for specialty, experience, litigation background, fee structure, credentials, location, and more.

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