Edward Carden
Country not established
- Devices
- 1
What Edward Carden makes
Edward Carden manufactures the CHIN UP, a Class I medical device designed for orthopedic use in spinal stabilization procedures. This product is intended for surgical applications where internal fixation is required, such as in spinal fusion surgeries.
The company’s portfolio is regulated under Class I medical devices in the United States, with relevant products listed via FDA 510(k) clearance. The manufacturer operates from the US, adhering to applicable regulatory standards for device authorization.
Catalogue
Chin Up Ref K943837
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Edward Carden have in the registry?
The registry currently lists 1 device for Edward Carden. Devices recorded under merged duplicate company entries are counted once.
Which registries list Edward Carden's devices?
Among its 1 most recently registered device, Edward Carden has devices listed in FDA 510(k) (1 device).
What risk classes do Edward Carden's devices fall under?
Among its 1 most recently registered device, the classes recorded for Edward Carden's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Edward Carden in the registry?
The most recently registered devices listed for Edward Carden include CHIN UP.