# K173319: KaVo NOMAD Pro 2 Handheld X-ray System

- Pathway: 510(k) (Special)
- Applicant: Aribex
- Decided: Nov 16, 2017 after 27 days
- Product code: EHD (Unit, X-Ray, Extraoral With Timer)
- Device class: 2
- Regulation: 21 CFR 872.1800
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K000061 (2000). 4 ancestors in all.
9 later devices descend from it; 8 cite it directly.
0 of 14 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K081664: Nomad Pro X-Ray System, Aribex, Inc. (2008) Summary page 4.

## Most influential descendants
- K221233: DT-703 (2022), 1 descendant of its own
- K260367: Portable Dental X-ray System Model PDX nova (2026), 0 descendants of its own
- K253864: NOMAD Pro 3 (2026), 0 descendants of its own
- K241305: LifeRay Intraoral Handheld X-ray System (2024), 0 descendants of its own
- K233914: XVbeam2000 (2024), 0 descendants of its own

## Indications for use
The KaVo NOMAD Pro 2 Handheld X-ray System is indicated for use only by a trained and qualified dentist or dental technician for both adult and pediatric subjects as an extraoral diagnostic dental X-ray source to produce X-ray images using intraoral image receptors.

Source page: https://510kreport.com/device/K173319
Methodology: https://510kreport.com/methodology