# Dentronix, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 9 (1977–1991): 9 510(k) clearances
- Product codes: FZT (5), HTZ (2), KMH (2)
- 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
- Coltene/Whaledent, Inc.: 1 (https://510kreport.com/company/coltene-whaledent)

## Its most-cited devices
- K880322: Dentronix DDS 5000 Dry Heat Sterilization System (1988), cited by 1

## Recent decisions
- K910202: Dentronix Model 2000 (Mar 13, 1991)
- K880322: Dentronix DDS 5000 Dry Heat Sterilization System (Jul 13, 1988)
- K771006: Modified Podiatry Products (Jun 17, 1977)
- K771005: New Podiatry Products (Jun 17, 1977)
- K770305: Cutter, P607 Bone (Mar 9, 1977)
- K770302: Cutter, P606 Bone (Mar 9, 1977)
- K770303: Nipper, Nail, P610 English (Mar 9, 1977)
- K770304: Cutter, P605 General Purpose (Mar 9, 1977)

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