# Verite

- Location (FDA's records): Mchenry, IL
- FDA decisions: 10 (1979–1985): 10 510(k) clearances
- Product codes: GZJ (6), IPF (3), GZI (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
- Neuromotion, Inc.: 1 (https://510kreport.com/company/neuromotion)

## Its most-cited devices
- K813515: Veri/DFS TM #817 (1982), cited by 1

## Recent decisions
- K844727: MODEL 1000 (Jul 9, 1985)
- K840099: Model 800-a Veri/PPR (Nov 28, 1984)
- K840098: Model 811 Veri/Tens & PO (Jul 17, 1984)
- K822929: Veril/PPR Personal Pain Reliever #800 (Nov 17, 1982)
- K820651: Model 860-1 Veri/Probe (Apr 29, 1982)
- K813108: Model 500 Veri/500 (Feb 19, 1982)
- K813515: Veri/DFS TM #817 (Jan 19, 1982)
- K811351: Veri-Fier (Jul 30, 1981)

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