# Viveve, Inc.

- Location (FDA's records): Englewood, CO
- FDA decisions: 3 (2016–2022): 3 510(k) clearances
- Product codes: GEI (3)
- 510(k) review time since 2016: median 32 days, against 108 for FDA's reviews in the same codes and years (3 of 3 faster)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 3 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Tivamed, Inc.: 1 (https://510kreport.com/company/tivamed)
- Viveve Medical, Inc.: 1 (https://510kreport.com/company/viveve-medical)

## Firms that cite its devices most
- Viveve Medical, Inc.: 2 (https://510kreport.com/company/viveve-medical)

## Its most-cited devices
- K180584: Viveve RF System, Secure (2018), cited by 2
- K162547: Viveve System (2016), cited by 1

## Recent decisions
- K213814: Viveve 2.0 System (Feb 2, 2022)
- K180584: Viveve RF System, Secure (Apr 6, 2018)
- K162547: Viveve System (Oct 6, 2016)

Source page: https://510kreport.com/company/viveve