Cyberex Corp.
United StatesFDA 510(k) applicant, unverified
- Devices
- 4
What Cyberex Corp. makes
Cyberex Corp. manufactures hemodialyzers, including the CYBER 120 and CYBER 80 models, designed for renal replacement therapy. The company also produces the REPGREEN Ultrafiltration Monitor, a device used to track fluid removal during dialysis procedures.
These products are classified as Class II medical devices under FDA regulations and are listed via the 510(k) pathway. Cyberex Corp. is based in the United States.
Catalogue
Cyber 120 Hemodialyzer Ref K802478
510(k) 510(k)Cyber 80 Hemodialyzer Ref K810837
510(k) 510(k)Repgreen Ultrafiltration Monitor Ref K790824
510(k) 510(k)Cyber 120 Hemodialyzer Ref K801377
510(k) 510(k)
Frequently asked questions
How many devices does Cyberex Corp. have in the registry?
The registry currently lists 4 devices for Cyberex Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cyberex Corp.'s devices?
Among its 4 most recently registered devices, Cyberex Corp. has devices listed in FDA 510(k) (4 devices).
What risk classes do Cyberex Corp.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Cyberex Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cyberex Corp. in the registry?
The most recently registered devices listed for Cyberex Corp. include CYBER 120 HEMODIALYZER, CYBER 80 HEMODIALYZER and REPGREEN ULTRAFILTRATION MONITOR.