# Vivus, Inc.

- Location (FDA's records): Mountain View, CA
- FDA decisions: 2 (1996–2000): 2 510(k) clearances
- Product codes: LKY (2)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K003115: Actis Adjustable Constriction Loop (Dec 19, 2000)
- K962915: Actis (Venous Flow Controller) (Dec 10, 1996)

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