Medical Devices Expert Witnesses in Wyoming

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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

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  • Review Fee $550/hr
    Court Fee $800/hr

    This expert is a world renowned Biomedical Engineer specializing in prosthetics. He received a BA in mathematics and a BAI in microelectronics and electrical engineering from Trinity College Dublin, Ireland, in 1983. After working as a control engineer in England, he moved to the USA and obtained his MS and PhD degrees in biomedical engineering from Northwestern University in Evanston, IL. He has extensive experience working with lower and upper limb prosthetics research. His recent research is focused on the development an artificial hand replacement capable of true dexterous manipulation for use by persons with upper-limb loss. He covers all aspects of the problem ranging from neural control and sensing, mechatronic design and development, novel actuator technologies, and clinical deployment of these systems. He is currently the Director of the Biomechatronics Development Laboratory at a university in CO. He is also a Research Healthcare Scientist for a VA Health Care System, and holds Research Associate Professor appointments in the Departments of Bioengineering and Physical Medicine & Rehabilitation.

    Research Healthcare Scientist, A VA Medical Center in CO

    Doctor of Philosophy (PhD), Northwestern University

    Lafayette,

    Colorado

    View profile

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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