# Dicon, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 4 (1981–1982): 4 510(k) clearances
- Product codes: HPT (3), HKO (1)
- 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
- K822580: Auto Periometer 3000 (Sep 30, 1982)
- K820877: Automatic Objective Refractor 2000 (Jun 25, 1982)
- K811346: Dicon Auto Perimeter 200 (Aug 20, 1981)
- K811347: Dicon Auto Perimeter 2000 (Aug 20, 1981)

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