Lleventon
SpainFDA applicant, unverified
- Devices
- 1
What Lleventon makes
Lleventon manufactures MONITRODE, a medical device designed for continuous patient monitoring in clinical settings.
The MONITRODE device is classified as Class II under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Monitrode Ref K903491
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lleventon have in the registry?
The registry currently lists 1 device for Lleventon. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lleventon's devices?
Among its 1 most recently registered device, Lleventon has devices listed in FDA 510(k) (1 device).
What risk classes do Lleventon's devices fall under?
Among its 1 most recently registered device, the classes recorded for Lleventon's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lleventon in the registry?
The most recently registered devices listed for Lleventon include MONITRODE.