Zimed Medikal
TürkiyeFDA 510(k) applicant, unverified
- Devices
- 1
What Zimed Medikal makes
Zimed Medikal manufactures orthopedic fixation systems, including the Distal Medial Tibial Plate and Screw System, designed for internal fixation of tibial fractures.
The company’s portfolio is regulated under FDA’s Class II device classification, with products listed via the 510(k) pathway. Zimed Medikal operates from the United States.
Catalogue
- 510(k) 510(k)
Frequently asked questions
How many devices does Zimed Medikal have in the registry?
The registry currently lists 1 device for Zimed Medikal. Devices recorded under merged duplicate company entries are counted once.
Which registries list Zimed Medikal's devices?
Among its 1 most recently registered device, Zimed Medikal has devices listed in FDA 510(k) (1 device).
What risk classes do Zimed Medikal's devices fall under?
Among its 1 most recently registered device, the classes recorded for Zimed Medikal's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Zimed Medikal in the registry?
The most recently registered devices listed for Zimed Medikal include Zimed Distal Medial Tibial Plate and Screw System.