According to GlobalData’s medical device pipeline database, 73 Aortic Stent Grafts devices are in various stages of development globally. GlobalData’s report Aortic Stent Grafts 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, 43 are in active development, while the remaining 30 are in an inactive stage of development. There are ten products in the early stages of development, and the remaining 33 are in the late stages of development.
Aortic Stent grafts are used to reinforce a weaken aorta to prevent ruptures. Aortic Stent Grafts can be of allografts or synthetic materials. Aortic stent grafts include abdominal aortic stent grafts and thoracic aortic stent grafts along with additional extensions. One unit refers to One aortic stent graft.
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 Aortic Stent Grafts 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 Aortic Stent Grafts devices. Overall, most of these Aortic Stent Grafts pipeline devices are being developed by private entities.
Key players involved in the active development of Aortic Stent Grafts include Endologix, Terumo Aortic, JOTEC, Medtronic, St. Jude Medical, Shanghai MicroPort Endovascular MedTech Group, Merit Medical Systems, Lombard Medical Technologies, Lundquist Institute and Cook Medical.
For a complete picture of the developmental pipeline for Aortic Stent Grafts 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.
