According to GlobalData’s medical device pipeline database, 18 Synthetic Tissue Sealants devices are in various stages of development globally. GlobalData’s report Synthetic Tissue Sealants provides an overview of the segment’s pipeline landscape and offers detailed analysis of its products. Buy the report here.
Of these devices, ten are in active development, while the remaining nine are in an inactive stage of development. There are six products in the early stages of development, and the remaining four are in the late stages of development.
Synthetic tissue sealants are made of chemical compounds that consist of a variety of artificial components such as polyethylene glycol, synthetic peptides, and protein polymers. One unit refers to 5ml vial of synthetic tissue sealant.
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 Synthetic Tissue Sealants 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 Synthetic Tissue Sealants devices. Overall, most of these Synthetic Tissue Sealants pipeline devices are being developed by private entities.
Key players involved in the active development of Synthetic Tissue Sealants include Polyganics, Cohera Medical, CR Bard, GATT Technologies, InVivo Therapeutics, Nurami Medical, Empa, Empa, Samyang Biopharmaceuticals and Tissium.
For a complete picture of the developmental pipeline for Synthetic Tissue Sealants devices, buy the report here.
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