# Cg Medtech Co., Ltd.

- Location (FDA's records): Uijeongbu-Si, KR
- FDA decisions: 2 (2025–2025): 2 510(k) clearances
- Product codes: NKG (1), MAX (1)
- Predicates its devices cite: 7 (0 its own); citations of its devices by later devices: 0 (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
- U&I Corporation: 3 (https://510kreport.com/company/u-i)
- Medtronic Sofamor Danek USA, Inc.: 2 (https://510kreport.com/company/medtronic-sofamor-danek-usa)
- Innosys Co., Ltd.: 1 (https://510kreport.com/company/innosys)
- Edisoninno Co., Ltd.: 1 (https://510kreport.com/company/edisoninno)

## Recent decisions
- K252351: UniSpace® TPLIF Cage (Oct 28, 2025)
- K251725: ANAX™ OCT Spinal System (Jun 25, 2025)

Source page: https://510kreport.com/company/cg-medtech