Trident Orthopedics
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- Devices
- 1
What Trident Orthopedics makes
Trident Orthopedics manufactures the Trident Extremity Fixation System, a medical device designed for internal fixation of long bone fractures, including those in extremities like the femur, tibia, and humerus. The system includes locking plates, screws, and intramedullary nails to stabilize bone fragments during the healing process, supporting surgical treatment for traumatic or pathological fractures.
The Trident Extremity Fixation System is classified as a Class II device under FDA regulations and requires a 510(k) clearance for market authorization. The company is based in the United States, and the device is listed in the FDA’s 510(k) database.
Catalogue
Trident Extremity Fixation System Ref K171690
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Trident Orthopedics have in the registry?
The registry currently lists 1 device for Trident Orthopedics. Devices recorded under merged duplicate company entries are counted once.
Which registries list Trident Orthopedics's devices?
Among its 1 most recently registered device, Trident Orthopedics has devices listed in FDA 510(k) (1 device).
What risk classes do Trident Orthopedics's devices fall under?
Among its 1 most recently registered device, the classes recorded for Trident Orthopedics's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Trident Orthopedics in the registry?
The most recently registered devices listed for Trident Orthopedics include Trident Extremity Fixation System.