# Syntex Dental Products, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 3 (1982–1983): 3 510(k) clearances
- Product codes: EKQ (1), EIA (1), DZS (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
- K832378: Vibratory Endodontic System (Oct 4, 1983)
- K823230: Sterile Water System (Dec 3, 1982)
- K822610: Precapsuled Dental Amalgam (Sep 14, 1982)

Source page: https://510kreport.com/company/syntex-dental-products