According to GlobalData’s medical device pipeline database, 17 Mechanical Heart Valves devices are in various stages of development globally. GlobalData’s report Mechanical 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, nine are in active development, while the remaining eight are in an inactive stage of development. There are four products in the early stages of development, and the remaining five are in the late stages of development.
Mechanical heart valves are generally made of non–physiological materials with a mobile occluder, which is made of rigid materials. This segment comprises of Mechanical Sutured Mitral Valve Replacements and Mechanical 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 Mechanical 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 Mechanical Heart Valves devices. Overall, most of these Mechanical Heart Valves pipeline devices are being developed by private entities.
Key players involved in the active development of Mechanical Heart Valves include Meril Life Sciences, Innovia, On-X Life Technologies, Indian Institute of Technology, Kanpur, Innovator Lab Consultants India, Artivion, Autus Valve Technologies, Shanghai Aoliu Medical Technology, TTK Healthcare and University of Pittsburgh Medical Center.
For a complete picture of the developmental pipeline for Mechanical 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.
