Stryker Corporation (Tornier, Inc.)
Country not established
- Devices
- 5
What Stryker Corporation (Tornier, Inc.) makes
The company manufactures orthopedic implants for humeral reconstruction, including modular systems for shoulder surgery such as the Tornier Humeral Reconstruction System and its stem components like the Tornier Perform Humeral System.
These devices are classified as Class II under FDA regulations and are authorised via the 510(k) pathway. The company is headquartered in the United States.
Catalogue
Tornier Perform Reversed Glenoid and Tornier Perform Reversed Augmented Glenoid Shoulder System Ref K260102
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Blueprint Patient-Specific Instrumentation Ref K253674
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Stryker Corporation (Tornier, Inc.) have in the registry?
The registry currently lists 5 devices for Stryker Corporation (Tornier, Inc.). Devices recorded under merged duplicate company entries are counted once.
Which registries list Stryker Corporation (Tornier, Inc.)'s devices?
Among its 5 most recently registered devices, Stryker Corporation (Tornier, Inc.) has devices listed in FDA 510(k) (5 devices).
What risk classes do Stryker Corporation (Tornier, Inc.)'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Stryker Corporation (Tornier, Inc.)'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Stryker Corporation (Tornier, Inc.) in the registry?
The most recently registered devices listed for Stryker Corporation (Tornier, Inc.) include Tornier Perform Reversed Glenoid and Tornier Perform Reversed Augmented Glenoid Shoulder System, Tornier Humeral Reconstruction System (Tornier HRS), Blueprint Patient-Specific Instrumentation and Blueprint Patient-Specific Instrumentation; Shoulder iD Primary Reversed Glenoid.