Accin Corporation
United StatesFDA applicant, unverified
- Devices
- 2
What Accin Corporation makes
Accin Corporation manufactures the Uni-Knee System, a Class II medical device designed for partial knee replacement surgery. This product is intended to restore function and alleviate pain in patients with degenerative joint conditions affecting the knee.
The Uni-Knee System is regulated under the FDA’s 510(k) pathway as a Class II device and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Accin Uni-Knee System Ref K060670
Regimes: 510(k) Registry: 510(k)Accin Uni-Knee System Ref K063782
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Accin Corporation have in the registry?
The registry currently lists 2 devices for Accin Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Accin Corporation's devices?
Among its 2 most recently registered devices, Accin Corporation has devices listed in FDA 510(k) (2 devices).
What risk classes do Accin Corporation's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Accin Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Accin Corporation in the registry?
The most recently registered devices listed for Accin Corporation include ACCIN UNI-KNEE SYSTEM.