Lantos Technologies
Country not established
- Devices
- 1
What Lantos Technologies makes
Lantos Technologies manufactures the Lantos 3D Ear Scanner, a device designed for creating three-dimensional digital impressions of the ear for custom molding or digital modeling applications.
The Lantos 3D Ear Scanner is classified as a Class I medical device in the U.S. and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Lantos 3D Ear Scanner Ref K121326
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lantos Technologies have in the registry?
The registry currently lists 1 device for Lantos Technologies. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lantos Technologies's devices?
Among its 1 most recently registered device, Lantos Technologies has devices listed in FDA 510(k) (1 device).
What risk classes do Lantos Technologies's devices fall under?
Among its 1 most recently registered device, the classes recorded for Lantos Technologies's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Lantos Technologies in the registry?
The most recently registered devices listed for Lantos Technologies include LANTOS 3D EAR SCANNER.