According to GlobalData’s medical device pipeline database, 50 Tissue Heart Valves devices are in various stages of development globally. GlobalData’s report Tissue Heart Valves 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, 24 are in active development, while the remaining 26 are in an inactive stage of development. There are 18 products in the early stages of development, and the remaining six are in the late stages of development.
Tissue heart valve are a combination of tissue and synthetic biomaterials with the tissue itself being flexible. Bovine and porcine valves are included here. This segment comprises Tissue Sutured Mitral Valve Replacements, Tissue Sutureless Aortic Valve Replacements and Tissue Sutured Aortic Valve Replacements.
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 Heart Valves 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 Heart Valves devices. Overall, most of these Tissue Heart Valves pipeline devices are being developed by private entities.
Key players involved in the active development of Tissue Heart Valves include CorMatrix Cardiovascular, Charles Stark Draper Laboratory, Meril Life Sciences, ValveXchange, University of California Irvine, Anchorvalve, Artivion, Edwards Lifesciences, enVVeno Medical and Colibri Heart Valve.
For a complete picture of the developmental pipeline for Tissue Heart Valves 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.
