Eska Implants GmbH
Country not established
- Devices
- 2
What Eska Implants GmbH makes
Eska Implants GmbH makes the ESKA Modular Hip System Cemented, a cemented modular hip prosthesis used in joint replacement surgery.
The ESKA Modular Hip System Cemented is a Class II medical device listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
Eska-Libur Hip Stem Ref K053557
Regimes: 510(k) Registry: 510(k)Eska Modular Hip System Cemented Ref K030867
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Eska Implants GmbH have in the registry?
The registry currently lists 2 devices for Eska Implants GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Eska Implants GmbH's devices?
Among its 2 most recently registered devices, Eska Implants GmbH has devices listed in FDA 510(k) (2 devices).
What risk classes do Eska Implants GmbH's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Eska Implants GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Eska Implants GmbH in the registry?
The most recently registered devices listed for Eska Implants GmbH include ESKA-LIBUR HIP STEM and ESKA MODULAR HIP SYSTEM CEMENTED.