# Dentec, Inc.

- Location (FDA's records): Walker, MI
- FDA decisions: 3 (1983–1990): 3 510(k) clearances
- Product codes: EAX (1), ETN (1), DYT (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
- K894930: Dentec 4000 (Mar 27, 1990)
- K864376: Fiberbond (Apr 7, 1987)
- K833429: Peri Mirror/Saliva Ejector (Dec 22, 1983)

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