Ebi Electro Biology
Country not established
- Devices
- 3
What Ebi Electro Biology makes
Ebi Electro Biology makes spinal implant systems, including the EBI Spinelink Anterior Cervical Spinal System and the EBI Omega 21 System, which are used for spinal fusion and stabilization procedures.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Ebi Spinelink Anterior Cervical Spinal System Ref K973923
Regimes: 510(k) Registry: 510(k)Ebi Omega 21 System Ref K991721
Regimes: 510(k) Registry: 510(k)Omega 21 System Ref K973683
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ebi Electro Biology have in the registry?
The registry currently lists 3 devices for Ebi Electro Biology. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ebi Electro Biology's devices?
Among its 3 most recently registered devices, Ebi Electro Biology has devices listed in FDA 510(k) (3 devices).
What risk classes do Ebi Electro Biology's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Ebi Electro Biology's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ebi Electro Biology in the registry?
The most recently registered devices listed for Ebi Electro Biology include EBI SPINELINK ANTERIOR CERVICAL SPINAL SYSTEM, EBI OMEGA 21 SYSTEM and OMEGA 21 SYSTEM.