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Showing 50 Of 141 records
Curved Posterior Lumbar Cage
A hollow implant that consists of a unique configuration of both solid and porous structures built using AMagine Technology, our proprietary approach to implant creation using additive manufacturing
Anterior Cervical Cage
A hollow implant that consists of a unique configuration of both solid and porous structures built using AMagine Technology, our proprietary approach to implant creation using additive manufacturing
Posterior Lumbar Cage
A hollow, rectangular implant that consists of a unique configuration of both solid and porous structures built using AMagine Technology, our proprietary approach to implant creation using additive manufacturing
OR integration platform
Our OR integration, with its intuitive workflow and safety features, allows nurses to focus on delivering the highest level of patient care rather than managing the nuances of the surgical space.
Acetabular System
Have confidence in a powerful combination–a system that builds on the legacy that has defined our Trident brand for more than two decades, paired with the latest additive manufactured Tritanium In-Growth Technology or PureFix HA.
Cementless Total Knee System
Cementless total knee arthroplasty (TKA) with Triathlon Tritanium is the latest evolution in the Triathlon knee portfolio. Triathlon Tritanium combines the kinematics of Triathlon with the latest in highly porous biologic fixation technology. Tritanium's innovative tibial baseplate and metal-backed patella components are SOMA-designed and enabled by Stryker's proprietary Additive Manufacturing technology.
Implants
We offer market-leading knee replacement implants for partial knee and total knee arthroplasty for primary and revision procedures featuring our cemented and cementless flagship TKA solution, the Triathlon Knee System.
Implants
We offer market-leading knee replacement implants for partial knee and total knee arthroplasty for primary and revision procedures featuring our cemented and cementless flagship TKA solution, the Triathlon Knee System.
A patient specific solution
Rigid internal fixation for primary and secondary mandible reconstruction.
Powered by Connected OR operating system
Our iSuite offers a combination of equipment and software that transform the traditional operating room into a modern, state-of-the-art surgical environment, empowering your surgical teams. We collaborate with you to understand your unique business needs for you to deliver best in class patient care. Design.Equip.Connect.
Single Portal Suture Passing System
The Champion Slingshot has been optimized for use in the shoulder and allows you to both pass and retrieve suture using a single portal. Its ergonomic thumb-slide design helps to eliminate additional procedural steps and potentially reduce operating time.
We are a global leader of complex spine and minimally invasive solutions focused on achieving three-dimensional Total Body Balance.
Our spine business unit offers one of the most comprehensive and diverse product portfolios, including our leading 3D-printed technologies, enabling surgeons to provide their patients with treatment options.
Our products include implants, instruments, and biologic solutions for the cervical, thoracic and lumbar spine.
Surgical table
The Operon D830 is designed to deliver on the increasing demand for flexibility in your operating room.
Software
CranialMap 3.0 Navigation Software is a simplified solution to incorporate navigation into neurosurgical procedures. From pre-op planning to intra-operative guidance and control, CranialMap 3.0 has been designed to meet the demands in today’s operating room and help deliver better patient outcomes. Advanced imaging visualization enables you to compare unaffected and affected anatomy with automatic symmetrical visualization as a pre- and intraoperative guide.
Live video conferencing platform powered by ConnectSuite
iSuite live video connects clinicians within the operating room to other ORs, pathology for lab verification, surgeons for intraoperative consultations, and to auditoriums for education.
Equipment management system
The Teletom equipment management system provides ceiling-mounted solutions to manage your surgical equipment, reducing reliance on carts and enabling you to streamline the workflow of your operating suites.
SpinePlex bone cement is a derivative of Simplex P bone cement and has an average working time of 10-12 minutes. It contains the same Polymethylmetacrylate (PMMA) and is manufactured using the same proprietary process.
Surgical light
Illuminate the surgical field in your operating suite with our Berchtold LED F Generation surgical light. Delivering maximum brightness and offering multiple configuration options, you can customize your lighting experience.
Integration system
The Connected OR IP system provides intuitive user control of your connected devices, creating a future-ready integration platform with scalable 4K video routing, designed to increase efficiency in your operating room and to make your job easier.
The U.S. Food and Drug Administration (FDA) created unique device identification, often abbreviated UDI, a rule that requires medical device manufacturers to update their products with a unique device identifier that includes both device and production identifiers (such as expiration date and lot or serial number).
Stabilization System
The Chesapeake Cervical-Ti Stabilization System is a multi-screw construct designed to provide stability to the anterior column while eliminating the need for supplemental fixation in the cervical spine. [1] Featuring SMARTLock Technology, the system exemplifies advances in new and innovative instrumentation.
Allows for accurate planning and precise clinical transfer via CAD/CAM splint technology.
Reprocessing of single-use medical devices (SUDs) is the practice of inspecting, cleaning, function testing, sterilizing and packaging so that they can be clinically and safely used again. Reprocessing of SUDs is regulated by the FDA. We satisfy all FDA regulatory requirements to reprocess medical devices and ensure that our reprocessed devices are substantially equivalent to original equipment devices.
Reprocessing of single-use medical devices (SUDs) is the practice of inspecting, cleaning, function testing, sterilizing and packaging so that they can be clinically and safely used again. Reprocessing of SUDs is regulated by the FDA. We satisfy all FDA regulatory requirements to reprocess medical devices and ensure that our reprocessed devices are substantially equivalent to original equipment devices.
A digital planning solution for maxillofacial surgical procedures.
Nailing System
Intramedullary nail for treating proximal femoral and diaphyseal femur fractures.