Wellvii, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Wellvii, Inc. makes
Wellvii, Inc. manufactures the VitalDetect device, a medical monitoring solution designed for real-time patient vital sign tracking, including heart rate and respiratory patterns.
The VitalDetect device is classified as a Class II medical device under FDA regulations and is listed via the 510(k) clearance pathway. The company is based in the United States.
Catalogue
BP Go (BPP-855) Ref K261061
Regimes: 510(k) Registry: 510(k)VitalDetect Ref K231625
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Wellvii, Inc. have in the registry?
The registry currently lists 2 devices for Wellvii, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Wellvii, Inc.'s devices?
Among its 2 most recently registered devices, Wellvii, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Wellvii, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Wellvii, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Wellvii, Inc. in the registry?
The most recently registered devices listed for Wellvii, Inc. include BP Go (BPP-855) and VitalDetect.