Jmea Corporation
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- Devices
- 1
What Jmea Corporation makes
Jmea Corporation manufactures the JMEA Cannulated Bone Screw System, a device designed for orthopedic fixation in bone surgery. The system features hollow screws that allow for the insertion of bone grafts or cement, facilitating enhanced stability during healing processes. It is intended for use in procedures requiring internal fixation, such as fracture stabilization or spinal applications.
The JMEA Cannulated Bone Screw System is classified as a Class II medical device under FDA regulations and has undergone 510(k) clearance. The product is listed in the FDA’s 510(k) database, adhering to U.S. regulatory requirements for orthopedic fixation devices. The company is headquartered in the United States.
Catalogue
Jmea Cannulated Bone Screw System Ref K080259
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Jmea Corporation have in the registry?
The registry currently lists 1 device for Jmea Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Jmea Corporation's devices?
Among its 1 most recently registered device, Jmea Corporation has devices listed in FDA 510(k) (1 device).
What risk classes do Jmea Corporation's devices fall under?
Among its 1 most recently registered device, the classes recorded for Jmea Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Jmea Corporation in the registry?
The most recently registered devices listed for Jmea Corporation include JMEA CANNULATED BONE SCREW SYSTEM.