Wonder Wire
Country not established
- Devices
- 2
What Wonder Wire makes
Wonder Wire manufactures orthodontic archwires and coated orthodontic devices.
The company is based in the United States, and its products are classified as Class I medical devices listed within the FDA 510(k) regulatory registry.
Catalogue
Coated Orthodontic Devices Ref K931631
Regimes: 510(k) Registry: 510(k)Orthodontic Arch Ref K872622
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Wonder Wire have in the registry?
The registry currently lists 2 devices for Wonder Wire. Devices recorded under merged duplicate company entries are counted once.
Which registries list Wonder Wire's devices?
Among its 2 most recently registered devices, Wonder Wire has devices listed in FDA 510(k) (2 devices).
What risk classes do Wonder Wire's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Wonder Wire's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Wonder Wire in the registry?
The most recently registered devices listed for Wonder Wire include COATED ORTHODONTIC DEVICES and ORTHODONTIC ARCH.