# Aribex, Inc.

- Location (FDA's records): Orem, UT
- FDA decisions: 4 (2005–2017): 4 510(k) clearances
- Names in FDA's records: Aribex, Inc. (3); Aribex (1)
- Product codes: EHD (3), IZL (1)
- Predicates its devices cite: 4 (2 its own); citations of its devices by later devices: 19 (2 its own)
- Recalls linked to its devices: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Minxray, Inc.: 1 (https://510kreport.com/company/minxray)
- Dentalez Group: 1 (https://510kreport.com/company/dentalez-group)

## Firms that cite its devices most
- VATECH Co., Ltd.: 2 (https://510kreport.com/company/vatech)
- Osstem Implant Co., Ltd.: 1 (https://510kreport.com/company/osstem-implant)
- Energy Resources International Co., Ltd. Hsinchu Branch: 1 (https://510kreport.com/company/energy-resources-international-co-hsinchu-branch)
- Oxos Medical, Inc.: 1 (https://510kreport.com/company/oxos-medical)
- Nanoray Co., Ltd.: 1 (https://510kreport.com/company/nanoray)
- Dental Imaging Technologies Corporation: 1 (https://510kreport.com/company/dental-imaging-technologies)
- Livermoretech, Inc.: 1 (https://510kreport.com/company/livermoretech)
- Dexco: 1 (https://510kreport.com/company/dexco)

## Its most-cited devices
- K173319: KaVo NOMAD Pro 2 Handheld X-ray System (2017), cited by 8
- K051795: Nomad Dental X-Ray System (2005), cited by 5
- K140723: Nomad MD 75K V Handheld X-Ray System (2014), cited by 3
- K081664: Nomad Pro X-Ray System (2008), cited by 3

## Recent decisions
- K173319: KaVo NOMAD Pro 2 Handheld X-ray System (Nov 16, 2017)
- K140723: Nomad MD 75K V Handheld X-Ray System (Aug 19, 2014)
- K081664: Nomad Pro X-Ray System (Jun 23, 2008)
- K051795: Nomad Dental X-Ray System (Jul 14, 2005)

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