# K060080: Diagnodent 2190 with Periodontal Probe

- Pathway: 510(k) (Special)
- Applicant: Kavo Dental Corporation
- Decided: Feb 8, 2006 after 29 days
- Product code: NTK (Light Transmission Caries Detector)
- Device class: 2
- Regulation: 21 CFR 872.1745
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to DEN980003 (1998). 6 ancestors in all.
27 later devices descend from it; 1 cites it directly.
0 of 34 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K042394: Diagnodent Perio Tip (Accessory), Kavo America Corporation (2005) Summary page 1.
- K051909: Diagnodent, Kavo America (2005) Summary page 1.

## Most influential descendants
- K073074: Key Laser Iii 1243 US with Detect (2008), 26 descendants of its own
- K101658: Waterlase MD Turbo Plus Model 7200XXX (2010), 25 descendants of its own
- K161669: Waterlase Express (2016), 21 descendants of its own
- K190319: Waterlase Laser System Family (2019), 19 descendants of its own
- K193656: SkyPulse (2020), 11 descendants of its own

## Indications for use
For use as an aid in the detection and localization of subgingival dental calculus.

Source page: https://510kreport.com/device/K060080
Methodology: https://510kreport.com/methodology