FDA Agents
Country not established
- Devices
- 1
What FDA Agents makes
The company manufactures orthodontic RAVE Composite Brackets, which are adhesive-mounted dental appliances used in fixed orthodontic treatment to align teeth.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The manufacturer is based in the United States.
Catalogue
Rave Composite Bracket Ref K052714
510(k) 510(k)
Frequently asked questions
How many devices does FDA Agents have in the registry?
The registry currently lists 1 device for FDA Agents. Devices recorded under merged duplicate company entries are counted once.
Which registries list FDA Agents's devices?
Among its 1 most recently registered device, FDA Agents has devices listed in FDA 510(k) (1 device).
What risk classes do FDA Agents's devices fall under?
Among its 1 most recently registered device, the classes recorded for FDA Agents's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from FDA Agents in the registry?
The most recently registered devices listed for FDA Agents include RAVE COMPOSITE BRACKET.