According to GlobalData’s medical device pipeline database, nine Tissue Sutureless Aortic Valve Replacements devices are in various stages of development globally. GlobalData’s report provides an overview of the segment’s pipeline landscape and offers detailed analysis of its products. Buy the report here.

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Of these devices, four are in active development, while the remaining five are in an inactive stage of development. All devices are in the early stages of development.

Replacement of the aortic heart valve using a biological prosthesis. They are made from a stented tissue valve that can be compressed to become smaller. The valve does not require sutures to stay in place. One unit refers to one tissue sutureless aortic valve replacement.

Innovations in the medical devices sector are linked to the development of new approaches, processes, or technologies for treating, diagnosing, and managing disease in response to demand from healthcare for better patient outcomes and reduce healthcare costs.

Based on an analysis of GlobalData’s Medical Intelligence Center pipeline product database, these actively developed Tissue Sutureless Aortic Valve Replacements pipeline devices are all expected to be approved within the next ten years.

Currently, private organizations, public entities and institutions are working on the development of Tissue Sutureless Aortic Valve Replacements devices. Overall, most of these Tissue Sutureless Aortic Valve Replacements pipeline devices are being developed by private entities.

Key players involved in the active development of Tissue Sutureless Aortic Valve Replacements include Charles Stark Draper Laboratory, Venus Haoyue Medtech, VueKlar Cardiovascular, Artivion, Boston Children's Hospital, Colibri Heart Valve, Daidalos Solutions and Medtronic.

For a complete picture of the developmental pipeline for Tissue Sutureless Aortic Valve Replacements devices, buy the report here.

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GlobalData, the leading provider of industry intelligence, provided the underlying data, research, and analysis used to produce this article. 

The medical devices pipeline data used in this article were obtained from the Medical Pipeline Products Database of GlobalData’s Medical Intelligence Center. The Pipeline Products database is a is a comprehensive source of information on medical devices, it covers 39K products which are in development stage and intended for diagnosis, treatment, and management of diseases/conditions/symptoms directly or indirectly. The pipeline products included in the database are sourced from reliable and authenticated sources, such as company websites, SEC filings, conference presentations, analyst presentations, news releases, clinical trial registries, and grants. The information is collected by following systematic research techniques and proprietary methodology.