Vignet, Inc.
Country not established
- Devices
- 1
What Vignet, Inc. makes
Vignet, Inc. develops the Vignet Telehealth Manager, a software platform designed to facilitate remote patient monitoring and virtual healthcare delivery, enabling secure communication and data exchange between clinicians and patients.
The company’s portfolio is regulated under FDA’s Class II device classification, with the Vignet Telehealth Manager authorised via the 510(k) pathway. The device is listed in the FDA’s 510(k) database, and the manufacturer is based in the United States.
Catalogue
Vignet Telehealth Manager Ref K113446
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vignet, Inc. have in the registry?
The registry currently lists 1 device for Vignet, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vignet, Inc.'s devices?
Among its 1 most recently registered device, Vignet, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Vignet, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Vignet, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vignet, Inc. in the registry?
The most recently registered devices listed for Vignet, Inc. include VIGNET TELEHEALTH MANAGER.