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.
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
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.
We offer knee replacement implants for partial and total knee arthroplasty for primary and revision procedures. Our implants feature our flagship cemented and cementless TKA solution, the Triathlon Knee 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.
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.
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.
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.
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.
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).
Our X3 polyethylene supports our total hip, knee and shoulder arthroplasty solutions. X3’s patented manufacturing process of sequential crosslinking uses three separate gamma irradiation doses with an annealing step after each.
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.  Featuring SMARTLock Technology, the system exemplifies advances in new and innovative instrumentation.
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.
Adherus AutoSpray and Adherus AutoSpray ET Dural Sealants are indicated for use in patients who are 13 years of age and older, as an adjunct to standard methods of dural repair, such as sutures, to provide watertight closure during cranial procedures.
The Chesapeake Anterior-Lumbar Stabilization System is a
multi-screw construct that is designed to provide stability to the anterior
column, while reducing the need for supplemental fixation.  This system offers a comprehensive range of sizes carefully designed to assist with the restoration of sagittal balance and disc height. Featuring tifix Locking Technology,
Chesapeake allows for appropriate implant placement required to achieve fusion.