Homevue Health Systems, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Homevue Health Systems, Inc. makes
Homevue Health Systems, Inc. manufactures the Homevue Monitoring System Model TD 2000, a device designed for continuous monitoring of wound conditions, and the Homevue Wound Monitoring System, which tracks and documents wound healing progress at home.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) clearance process. The company is based in the United States.
Catalogue
Homevue Monitoring Sys.model Td 2000 Ref K912138
Regimes: 510(k) Registry: 510(k)Homevue Wound Monitoring System Ref K945807
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Homevue Health Systems, Inc. have in the registry?
The registry currently lists 2 devices for Homevue Health Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Homevue Health Systems, Inc.'s devices?
Among its 2 most recently registered devices, Homevue Health Systems, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Homevue Health Systems, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Homevue Health Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Homevue Health Systems, Inc. in the registry?
The most recently registered devices listed for Homevue Health Systems, Inc. include HOMEVUE MONITORING SYS.MODEL TD 2000 and HOMEVUE WOUND MONITORING SYSTEM.