Vitls, Inc.
Country not established
- Devices
- 1
What Vitls, Inc. makes
Vitls, Inc. develops the Vitls Platform, a software-as-a-medical-device solution designed for remote patient monitoring and clinical data aggregation in healthcare settings.
The company’s portfolio is regulated under FDA 510(k) clearance as Class II devices and is listed in the FDA’s 510(k) database. Vitls, Inc. is headquartered in the United States.
Catalogue
Vitls Platform Ref K191620
510(k) 510(k)
Frequently asked questions
How many devices does Vitls, Inc. have in the registry?
The registry currently lists 1 device for Vitls, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vitls, Inc.'s devices?
Among its 1 most recently registered device, Vitls, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Vitls, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Vitls, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vitls, Inc. in the registry?
The most recently registered devices listed for Vitls, Inc. include Vitls Platform.