According to GlobalData’s medical device pipeline database, 17 Internal Surgical Stapling Devices devices are in various stages of development globally. GlobalData’s report Internal Surgical Stapling Devices 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, six are in active development, while the remaining 11 are in an inactive stage of development. All devices are in the early stages of development.

Surgeons use Internal surgical stapling devices to apply staples that hold internal tissues together following various procedures. Internal surgical stapling devices include Open surgical stapling devices and Endoscopic surgical stapling devices, the latter of which is sometimes referred to as “Endocutters”.

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 Internal Surgical Stapling Devices 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 Internal Surgical Stapling Devices devices. Overall, most of these Internal Surgical Stapling Devices pipeline devices are being developed by private entities.

Key players involved in the active development of Internal Surgical Stapling Devices include Shenzhen Edge Medical, Chaim Sheba Medical Center, University of South Florida, Aesculap, Bolder Surgical, Covidien, Epic MD, ES Vascular, Ethicon Endo-Surgery and Intuitive Surgical.

For a complete picture of the developmental pipeline for Internal Surgical Stapling Devices 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.