Eska America Corp.
Country not established
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Eska Modular Hip System Acetabular Components Ref K021878
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Eska America Corp. have in the registry?
The registry currently lists 1 device for Eska America Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Eska America Corp.'s devices?
Among its 1 most recently registered device, Eska America Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Eska America Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Eska America Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Eska America Corp. in the registry?
The most recently registered devices listed for Eska America Corp. include ESKA MODULAR HIP SYSTEM ACETABULAR COMPONENTS.