According to GlobalData’s medical device pipeline database, five Primary Cementless Knee Replacement devices are in various stages of development globally. GlobalData’s report Primary Cementless Knee Replacement 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, four are in active development, while the remaining one is in an inactive stage of development. There are one products in the early stages of development, and the remaining three are in the late stages of development.
Orthopedic devices are medical devices that are used to treat or prevent musculoskeletal disorders. Primary Cementless Knee Replacement (PCLR) is a surgical procedure that replaces the damaged knee joint with artificial components. In a cementless knee replacement, the artificial components are designed to osseointegrate, or grow into the bone, without the use of cement. This allows for a more natural movement and function of the knee joint.
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 Primary Cementless Knee Replacement 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 Primary Cementless Knee Replacement devices. Overall, most of these Primary Cementless Knee Replacement pipeline devices are being developed by private entities.
Key players involved in the active development of Primary Cementless Knee Replacement include ConforMIS, Monogram Orthopaedics and Smith & Nephew.
For a complete picture of the developmental pipeline for Primary Cementless Knee Replacement 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.
