# American Dentronics, Inc.

- Location (FDA's records): Las Vegas, NV
- FDA decisions: 4 (1994–1998): 4 510(k) clearances
- Product codes: JEQ (3), LCN (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
- Kea Products, Ltd.: 1 (https://510kreport.com/company/kea-products)

## Its most-cited devices
- K980075: Cybersonic (1998), cited by 1

## Recent decisions
- K980075: Cybersonic (Mar 4, 1998)
- K935150: Soniplak (May 18, 1994)
- K935149: Sonibrush (Jan 31, 1994)
- K935148: Sonifloss (Jan 31, 1994)

Source page: https://510kreport.com/company/american-dentronics