# Vesta, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 4 (1979–1983): 4 510(k) clearances
- Product codes: BTQ (3), KOD (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

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

## Its most-cited devices
- K792018: Silicone Rubber-BI Nasopharyngeal Air (1979), cited by 1

## Recent decisions
- K834078: Silicone Rugger Disposable Yoke-Cpap (Dec 27, 1983)
- K810960: Nasopharyngeal Airway (Apr 23, 1981)
- K792719: 3 Way Urethral Irrigation Catheter (Jan 16, 1980)
- K792018: Silicone Rubber-BI Nasopharyngeal Air (Nov 13, 1979)

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