# Viveve Medical, Inc.

- Location (FDA's records): Englewood, CO
- FDA decisions: 4 (2019–2021): 4 510(k) clearances
- Names in FDA's records: Viveve Medical, Inc. (3); Viveve Medical (1)
- Product codes: GEI (4)
- 510(k) review time since 2016: median 66 days, against 105 for FDA's reviews in the same codes and years (2 of 4 faster)
- Predicates its devices cite: 6 (4 its own); citations of its devices by later devices: 5 (4 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
- Viveve, Inc.: 2 (https://510kreport.com/company/viveve)

## Firms that cite its devices most
- Viveve, Inc.: 1 (https://510kreport.com/company/viveve)

## Its most-cited devices
- K190422: Viveve System 2.0 (2019), cited by 2
- K193611: Viveve 2.0 System (2020), cited by 1
- K212678: Viveve System, Viveve 2.0 System (2021), cited by 1
- K200472: Viveve System (2020), cited by 1

## Recent decisions
- K212678: Viveve System, Viveve 2.0 System (Sep 14, 2021)
- K200472: Viveve System (Nov 18, 2020)
- K193611: Viveve 2.0 System (Jan 16, 2020)
- K190422: Viveve System 2.0 (Jun 12, 2019)

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