Ivoclar Vivadent, Agin
Country not established
- Devices
- 1
What Ivoclar Vivadent, Agin makes
Ivoclar Vivadent, Agin manufactures IPS E. MAX PRESS abutment solutions for Nobel Biocare, which are dental prosthetic components used in implant-supported restorations.
The company's products are classified as Class II medical devices and are listed in the FDA 510(k) registry. Ivoclar Vivadent, Agin is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ivoclar Vivadent, Agin have in the registry?
The registry currently lists 1 device for Ivoclar Vivadent, Agin. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ivoclar Vivadent, Agin's devices?
Among its 1 most recently registered device, Ivoclar Vivadent, Agin has devices listed in FDA 510(k) (1 device).
What risk classes do Ivoclar Vivadent, Agin's devices fall under?
Among its 1 most recently registered device, the classes recorded for Ivoclar Vivadent, Agin's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ivoclar Vivadent, Agin in the registry?
The most recently registered devices listed for Ivoclar Vivadent, Agin include IPS E. MAX PRESS ABUTMENT SOLUTIONS FOR NOBEL BIOCARE.