# Neks Technologies, Inc.

- Location (FDA's records): Laval, Quebec, CA
- FDA decisions: 3 (2003–2007): 3 510(k) clearances
- Names in FDA's records: Neks Technologies, Inc. (2); Neks Technologies (1)
- Product codes: NBL (2), EJB (1)
- Predicates its devices cite: 9 (3 its own); citations of its devices by later devices: 4 (3 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Kavo America: 3 (https://510kreport.com/company/kavo-america)
- Electro-Optical Sciences, Inc.: 1 (https://510kreport.com/company/electro-optical-sciences)
- Diamond General Development Corp.: 1 (https://510kreport.com/company/diamond-general-development)
- Dentalview, Inc.: 1 (https://510kreport.com/company/dentalview)

## Firms that cite its devices most
- Kavo America: 1 (https://510kreport.com/company/kavo-america)

## Its most-cited devices
- K023367: Detectar, Model N123-MI (2003), cited by 3
- K043156: D-Carie, Model N121-M1 (2005), cited by 1

## Recent decisions
- K063321: D-Carie/Detectar, Models N121, N123, N133, N134, N135 & N138 (Mar 30, 2007)
- K043156: D-Carie, Model N121-M1 (Apr 28, 2005)
- K023367: Detectar, Model N123-MI (Jun 25, 2003)

Source page: https://510kreport.com/company/neks-technologies