Viveve, Inc.
United StatesFDA applicant, unverified
Viveve, Inc. is a medical device manufacturer, with 16 devices listed in FDA GUDID and FDA 510(k) (FDA Class II) as of 13 Nov 2026.
- Devices
- 16
Registry facts
- Registries
- FDA GUDID 13
- FDA 510(k) 3
- Device classes
- FDA Class II 16
- Identifiers
- DUNS 025398094
Catalogue
Search and filter all 16 devicesCompany details
- DUNS number
- 025398094
Frequently asked questions
How many devices does VIVEVE, INC. have in the registry?
The registry currently lists 16 devices for VIVEVE, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list VIVEVE, INC.'s devices?
Among its 16 most recently registered devices, VIVEVE, INC. has devices listed in FDA 510(k) (3 devices) and FDA GUDID (13 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do VIVEVE, INC.'s devices fall under?
Among its 16 most recently registered devices, the classes recorded for VIVEVE, INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from VIVEVE, INC. in the registry?
The most recently registered devices listed for VIVEVE, INC. include VIVEVE Power Cord VIVPC0X, VIVEVE Hand Piece VIVHP01, 8 cm Treatment Tip VIVTT07 and CRYOGEN CANISTER VIVCC03.