# Kavo Dental Corporation

- Location (FDA's records): Deer Field, IL
- FDA decisions: 2 (2006–2021): 2 510(k) clearances
- Names in FDA's records: Kavo Dental Corporation (1); Kavo Dental GmbH (1)
- Product codes: NTK (1), EGS (1)
- Predicates its devices cite: 3 (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 whose devices it cites most
- Kavo America: 2 (https://510kreport.com/company/kavo-america)
- Kaltenbach & Voigt GmbH: 1 (https://510kreport.com/company/kaltenbach-voigt)

## Firms that cite its devices most
- Kavo America: 1 (https://510kreport.com/company/kavo-america)

## Its most-cited devices
- K060080: Diagnodent 2190 with Periodontal Probe (2006), cited by 1

## Recent decisions
- K213139: SURGmatic S15 L Pro (Dec 21, 2021)
- K060080: Diagnodent 2190 with Periodontal Probe (Feb 8, 2006)

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