Prodeon Medical, Inc.
Kimberly Marquez has a strong background in quality assurance and regulatory affairs. Kimberly currently holds the position of Vice President of Quality Assurance and Regulatory Affairs at Prodeon Medical. Prior to this, they worked at ASAHI Medical Technologies in a quality assurance role for five years. Kimberly also has experience in quality assurance and regulatory affairs at Alacrity Medical Systems, LLC and Previvo Genetics, Inc. Additionally, they served as Vice President of Quality Assurance at Cirtec Medical and held the position of Director of Quality Assurance at Circle Medical Devices. Kimberly started their career as a Program Manager at M2 Medical and later worked as a Commodity Manager at both Boston Scientific and Guidant. Kimberly also has experience as a Project Manager at ePeople.
Kimberly Marquez has attended Michigan State University, but specific details regarding the start year, end year, degree name, and field of study are not available.
Prodeon Medical, Inc.
Our program was initially started in 2016 with the mission of reimagining how men can be more easily treated for one of the most common disease states in the world affecting men, Benign Prostatic Hyperplasia (BPH). Prodeon Medical, Inc. has developed and is investigating a minimally invasive and patient-friendly approach to treating Lower Urinary Tract Symptoms (LUTS) due to BPH The procedure, known as the PURE™ (Prostatic Urethral REshaping) procedure uses the investigational the Urocross™ Expander System and Retrieval Sheath to relieve symptoms associated with BPH. Caution: The Urocross Expander System and Retrieval Sheath are for investigational use only under the Expander-2 Clinical Trial (NCT: 05400980) and are not for sale in the U.S. or outside the U.S.