Not currently registered with FDA under this name
Aribex
Charlotte, NC, United States. Named as applicant on 3 dental 510(k) clearances between 2005 and 2017. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 32005–2017
- Markets registered in
- 33 registrations outside the US
- Establishments
- 0—
510(k) clearances per year, 2000–2026
Registered in 3 markets
Where regulators' registries name Aribex as the manufacturer or the registration holder of a device.
| Market | Regulator | Named as | Name on the registry | Registrations | Issued | Records |
|---|---|---|---|---|---|---|
| United States | FDA | Applicant | Aribex | 3 clearances | 2005–2017 | Below |
| Saudi Arabia | SFDA | Manufacturer | Aribex, Inc. | 2 | — | Pure Global AI |
| Taiwan | TFDA | Manufacturer | Aribex | 1 | 2015–2015 | Pure Global AI |
Outside the US the count is of all the company's device registrations in that market, dental or not · matched by company name and country · registry data read 12 Nov 2026
510(k) clearances
Clearances on which FDA names Aribex as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 16 Nov 2017 | K173319 | KaVo NOMAD Pro 2 Handheld X-ray System | EHD Extraoral with Timer X-Ray Unit |
| 23 Jun 2008 | K081664 | NOMAD PRO X-RAY SYSTEM | EHD Extraoral with Timer X-Ray Unit |
| 14 Jul 2005 | K051795 | NOMAD DENTAL X-RAY SYSTEM | EHD Extraoral with Timer X-Ray Unit |
Some of these clearances are listed with FDA today by another company: Nobel Biocare Services AG (1), Dental Imaging Technologies Corporation (1).
Sources
FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record of the most recent filing, which can be a US agent.