Rogers Sciences, Inc.
Country not established
- Devices
- 1
What Rogers Sciences, Inc. makes
Rogers Sciences, Inc. makes the LUMINA 24, a medical device used for diagnostic or monitoring purposes in clinical settings.
The LUMINA 24 is classified as a Class II device and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Lumina 24 Ref K140386
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Rogers Sciences, Inc. have in the registry?
The registry currently lists 1 device for Rogers Sciences, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Rogers Sciences, Inc.'s devices?
Among its 1 most recently registered device, Rogers Sciences, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Rogers Sciences, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Rogers Sciences, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Rogers Sciences, Inc. in the registry?
The most recently registered devices listed for Rogers Sciences, Inc. include LUMINA 24.