According to GlobalData’s medical device pipeline database, 38 Cataract Surgery Devices devices are in various stages of development globally. GlobalData’s report Cataract Surgery 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, 13 are in active development, while the remaining 25 are in an inactive stage of development. There are ten products in the early stages of development, and the remaining three are in the late stages of development.
Cataract surgery is the removal of the natural lens of the eye that has developed an opacification and is then replacing it with an artificial intraocular lens to restore transparency. The most common procedure is called extra capsular cataract extraction (ECCE). This category includes ophthalmic viscoelastic devices (OVD).
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 Cataract Surgery 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 Cataract Surgery Devices devices. Overall, most of these Cataract Surgery Devices pipeline devices are being developed by private entities.
Key players involved in the active development of Cataract Surgery Devices include Bausch & Lomb, Alcon, Altacor, Advanced Refractive Technologies, Carl Zeiss Meditec, Centricity Vision, Cirle, ClearSight Innovations, Dutch Ophthalmic Research Center International and Edinburgh Biosciences.
For a complete picture of the developmental pipeline for Cataract Surgery 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.
