Viadent
Country not established
- Devices
- 1
What Viadent makes
Viadent manufactures the Professional Model 7525 Delivery System, a Class I dental device designed for precise application of dental materials in clinical settings.
The device is regulated under the FDA’s 510(k) pathway as a Class I medical device and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Professional Model 7525 Delivery System Ref K882759
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Viadent have in the registry?
The registry currently lists 1 device for Viadent. Devices recorded under merged duplicate company entries are counted once.
Which registries list Viadent's devices?
Among its 1 most recently registered device, Viadent has devices listed in FDA 510(k) (1 device).
What risk classes do Viadent's devices fall under?
Among its 1 most recently registered device, the classes recorded for Viadent's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Viadent in the registry?
The most recently registered devices listed for Viadent include PROFESSIONAL MODEL 7525 DELIVERY SYSTEM.