According to GlobalData’s medical device pipeline database, 19 Thoracic Aortic Stent Grafts devices are in various stages of development globally. GlobalData’s report Thoracic 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, 14 are in active development, while the remaining five are in an inactive stage of development. There are three products in the early stages of development, and the remaining 11 are in the late stages of development.
Thoracic aortic stent grafts are used to treat thoracic aortic aneurysms by reinforcing a part of the aorta using a minimally invasive procedure. One unit of thoracic aortic stent graft refers to a single main component (main proximal component) with no extensions.
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 Thoracic 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 Thoracic Aortic Stent Grafts devices. Overall, most of these Thoracic Aortic Stent Grafts pipeline devices are being developed by private entities.
Key players involved in the active development of Thoracic Aortic Stent Grafts include Terumo Aortic, JOTEC, Medtronic, Sree Chitra Tirunal Institute for Medical Sciences & Technology, St. Jude Medical, Lombard Medical Technologies, APT Medical, Artivion, Beijing Tianzhu Ruichang Medical Technology and EndoSpan.
For a complete picture of the developmental pipeline for Thoracic 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.
