Intradys
FranceFDA applicant, unverified
- Devices
- 1
What Intradys makes
Intradys manufactures the LUMYS (V1), a medical device designed for use in specific diagnostic or therapeutic procedures, though the exact application is not specified in the provided data.
The LUMYS (V1) is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Lumys (V1) Ref K243069
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Intradys have in the registry?
The registry currently lists 1 device for Intradys. Devices recorded under merged duplicate company entries are counted once.
Which registries list Intradys's devices?
Among its 1 most recently registered device, Intradys has devices listed in FDA 510(k) (1 device).
What risk classes do Intradys's devices fall under?
Among its 1 most recently registered device, the classes recorded for Intradys's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Intradys in the registry?
The most recently registered devices listed for Intradys include LUMYS (V1).