Not currently registered with FDA under this name
Neks Technologies, Inc.
Laval, Quebec, Canada. Named as applicant on 3 dental 510(k) clearances between 2003 and 2007. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 32003–2007
- Markets registered in
- 1United States
- Establishments
- 0—
510(k) clearances per year, 2000–2026
510(k) clearances
Clearances on which FDA names Neks Technologies, Inc. as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 30 Mar 2007 | K063321 | D-CARIE/DETECTAR, MODELS N121, N123, N133, N134, N135 & N138 | NBL Light-Induced Fluorescence Caries Detector |
| 28 Apr 2005 | K043156 | D-CARIE, MODEL N121-M1 | NBL Light-Induced Fluorescence Caries Detector |
| 25 Jun 2003 | K023367 | DETECTAR, MODEL N123-MI | EJB Dental Instrument Handle |
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.