# LK Consulting Group USA, Inc.

- Location (FDA's records): Fullerton, CA
- FDA decisions: 3 (2014–2015): 3 510(k) clearances
- Product codes: DZE (2), LLZ (1)
- Predicates its devices cite: 5 (0 its own); citations of its devices by later devices: 1 (0 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
- Kj Meditech Co., Ltd.: 2 (https://510kreport.com/company/kj-meditech)
- Nobel Biocare USA, LLC: 1 (https://510kreport.com/company/nobel-biocare-usa)
- Ewoosoft Co., Ltd.: 1 (https://510kreport.com/company/ewoosoft)
- Zest Anchors, Inc.: 1 (https://510kreport.com/company/zest-anchors)

## Firms that cite its devices most
- Ewoosoft Co., Ltd.: 1 (https://510kreport.com/company/ewoosoft)

## Its most-cited devices
- K150747: EzDent-i /E2/Prora View (2015), cited by 1

## Recent decisions
- K150747: EzDent-i /E2/Prora View (Apr 2, 2015)
- K130694: JR Implant System (Jun 19, 2014)
- K132144: Kerator (Mar 21, 2014)

Source page: https://510kreport.com/company/lk-consulting-group-usa