Viveve Medical, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 4
What Viveve Medical, Inc. makes
Viveve Medical, Inc. manufactures the Viveve System and the Viveve 2.0 System, which are medical devices designed for use in gynecological procedures.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) database. The company is based in the United States.
Catalogue
Viveve 2.0 System Ref K193611
510(k) 510(k)Viveve System Ref K200472
510(k) 510(k)Viveve System 2.0 Ref K190422
510(k) 510(k)Viveve System, Viveve 2.0 System Ref K212678
510(k) 510(k)
Frequently asked questions
How many devices does Viveve Medical, Inc. have in the registry?
The registry currently lists 4 devices for Viveve Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Viveve Medical, Inc.'s devices?
Among its 4 most recently registered devices, Viveve Medical, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Viveve Medical, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Viveve Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Viveve Medical, Inc. in the registry?
The most recently registered devices listed for Viveve Medical, Inc. include Viveve 2.0 System, Viveve System, Viveve System 2.0 and Viveve System, Viveve 2.0 System.