Dennis C. Gucciardo counsels domestic and global medical device manufacturers to help ensure they are operating in compliance with the myriad of US Food and Drug Administration (FDA) regulations, requirements, and expectations. He works with companies—from small startups to large multinational corporations—throughout the product life-cycle on how to bring novel technologies to market, maintain compliance, and avoid FDA enforcement actions.
Dennis helps companies bring medical devices to market, including navigating the premarket process, establishing a quality system, and complying with postmarket requirements.
When FDA action does occur, Dennis works with companies to develop risk-based and right-sized action plans to address FDA concerns, including responding to FDA Form 483 inspectional observations, untitled letters, and FDA warning letters; FDA-requested certified audit programs; and preparing medical device recall plans. When multiple sites are implicated, Dennis assists in preparing and executing global remediation plans to help ensure that all company sites act in accordance with company expectations and FDA requirements.
Dennis also assists in the defense of criminal investigations and conducts internal investigations of alleged regulatory violations. Additionally, he works with device companies in conducting regulatory due diligence and negotiating corporate mergers and acquisitions. He has been involved in numerous transactions ranging from multibillion-dollar acquisitions to the negotiation of supply and distribution agreements.
Dennis is a frequent speaker on regulatory compliance and enforcement issues in the device industry, and his pro bono work involves representing inmates before the US Parole Commission as part of the Washington Lawyers’ Committee DC Prisoners’ Project.
Before joining Morgan Lewis, Dennis was counsel at another global law firm.
Assisted a nontraditional medical device company with bringing its first medical device to market
Assisted in preparing a complex premarket notification, and responding to FDA feedback, concerning a medical device that was the subject of a CDC Health Alert
Reviewed advertising and promotional materials for compliance with FDA and FTC regulations
Assisted in the response to an FDA warning letter issued to a global company regarding alleged quality system and medical device reporting violations
Conducted a review of changes made to a premarket approval (PMA) manufacturing device since approval and prepared remedial submissions
Assisted in defending a company before a government investigation of a high-profile subject
Assisted companies with the diligence and acquisition of medical device manufacturers
Provided counsel on the development, implementation, and maintenance of compliant manufacturing and quality system processes that were innovative and practical
Assisted in the preparation for, and defense of, international inspection in follow up to import ban
Assisted in the successful resolution of an importation issue where FDA was preventing product from entering the United States
Developed and assisted in the execution of a global recall
University of Florida Levin College of Law, 2009, J.D., magna cum laude, Order of the Coif
University of Florida, 2005, B.S., summa cum laude
University of Florida, 2005, B.A., cum laude
District of Columbia
Awards and Affiliations
Executive Editor, Florida Law Review, University of Florida