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US: CAUTION – Investigational Device. Limited by Federal (or United States) law to investigational use.
Press

JenaValve Appoints Ken MacLeod, Ph.D. to Board of Directors

JenaValve

IRVINE, Calif., April 30, 2023

JenaValve Technology, Inc., developer and manufacturer of differentiated transcatheter aortic valve replacement (TAVR) systems, today announced that it has appointed Ken MacLeod, Ph.D., life sciences and medical device industry veteran, to its Board of Directors.

Dr. MacLeod has over 35 years of experience in the life sciences and medical devices industries and is currently a partner at Rosetta Capital, a venture capital firm focused on the life sciences and medical devices. Previously, he held senior operating roles in healthcare companies such as Abbott Laboratories and Serono SA. He has held life science fund management roles at SV Health Investors, Paul Capital, and Visium Healthcare Partners. Dr. MacLeod also serves on the board of Oxular Limited and has held previous board roles at Pharming Group N.V. (NASDAQ: PHAR) and On-X Life Technologies, Inc., a mechanical heart valve company acquired by Cryogenics Inc. (now NASDAQ: AORT).

“We are very pleased to welcome Ken to the JenaValve Board of Directors,” said John Kilcoyne, Chief Executive Officer. “His extensive background across life sciences and medical device operations and execution, as well as investing will bring valuable, additional perspective to our team.”

Dr. MacLeod earned his Bachelor of Science in Biological Sciences from the University of Manchester, and his Doctorate of Philosophy from the University of York.

Dr. MacLeod stated, “I am honored to join JenaValve as the company continues on its mission to treat patients suffering from heart valve disease, including symptomatic, severe aortic regurgitation and stenosis. I look forward to bringing my experience to help the company navigate the challenges and, more importantly, the immense opportunities ahead.”

About JenaValve

JenaValve Technology, Inc. is a medical device company focused on the design, development, and commercialization of innovative transcatheter heart valve solutions for the treatment of patients suffering from heart valve disease. The Company’s Trilogy® Heart Valve System is a transcatheter aortic valve replacement (TAVR) system designed to treat patients with symptomatic, severe aortic regurgitation (ssAR) and symptomatic, severe aortic stenosis (ssAS) in high surgical risk patients. The Trilogy System received CE Mark approval in May 2021, providing European physicians with the first TAVR device with true dual-disease treatment capabilities.

JenaValve received Breakthrough Device Designation from the FDA to facilitate the review of ALIGN-AR, a pivotal trial in the U.S., as part of its PMA application for the Trilogy Heart Valve System for the treatment of ssAR in high surgical risk patients. If approved, the Trilogy System would become the first and only TAVR system in the U.S. indicated for the treatment of AR.

JenaValve is headquartered in Irvine, California, with additional locations in Leeds, U.K., and Munich, Germany.

JenaValve is backed by Bain Capital Life Sciences, Andera Partners (formerly Edmond de Rothschild Investment Partners), Valiance Life Sciences, Rosetta Capital, Cormorant Asset Management, Legend Capital, NeoMed Management, RMM, VI Partners, Pictet Alternative Advisors SA, Qatar Investment Authority (QIA), Innovatus Capital Partners, and Peijia Medical Limited.

US: CAUTION – Investigational device. Limited by Federal (or United States) law to investigational use.

Additional information is available at www.jenavalve.com.

Investor Relations Contact:
Marissa Bych
marissa@gilmartinir.com

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The information in this Reimbursement Guide is provided for educational purposes only and is not intended to be coding or billing advice. This coding information is based upon publicly available information and is current as of April 1, 2026 and subject to change without notice. JenaValve Technology, Inc. cannot guarantee that any product or service billed with the codes listed will be covered or, if covered, the listed payment amount will be paid by any payer. It is the responsibility of the provider to select appropriate codes for each patient and to submit appropriate codes, charges, and modifiers for services rendered. Providers should contact insurers to verify correct coding procedures prior to submitting claims related to the use of JenaValve products. In all cases, providers must bill according to the rules, policies and procedures of individual payers. The medical record should document that the product or procedure was medically necessary and furnished or performed as reported. Clinical need, not reimbursement amount, should always drive clinical decision making. If you have any questions about appropriate billing for products or services, please consult your local payer. The information contained in this guide is provided to assist providers in understanding the reimbursement process. It is intended to assist providers in obtaining accurate and appropriate reimbursement for the healthcare services provided. It is not intended to increase or maximize reimbursement by any payer. It is strongly recommended that providers consult with their payer organizations with regard to local reimbursement policies. The information contained herein is provided for information purposes only and represents no statement, promise, or guarantee by JenaValve Technology, Inc. concerning levels of reimbursement, payment, or charge. Similarly, all CPT codes are supplied for information purposes only and represent no statement, promise, or guarantee by JenaValve Technology, Inc. that these codes will be appropriate or that reimbursement will be made. For additional information, please contact us at reimbursement.usa@jenavalve.com.