Wilde Dental (USA)
Country not established
- Devices
- 1
What Wilde Dental (USA) makes
Wilde Dental manufactures the CONVERTRAY modification, a dental device designed for clinical use.
The device is classified as Class II and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Convertray, Modification Ref K912001
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Wilde Dental (Usa) have in the registry?
The registry currently lists 1 device for Wilde Dental (Usa). Devices recorded under merged duplicate company entries are counted once.
Which registries list Wilde Dental (Usa)'s devices?
Among its 1 most recently registered device, Wilde Dental (Usa) has devices listed in FDA 510(k) (1 device).
What risk classes do Wilde Dental (Usa)'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Wilde Dental (Usa)'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Wilde Dental (Usa) in the registry?
The most recently registered devices listed for Wilde Dental (Usa) include CONVERTRAY, MODIFICATION.