# Chungwoo Co., Ltd.

- Location (FDA's records): Seoul, KR
- FDA decisions: 2 (2023–2024): 2 510(k) clearances
- Product codes: GEI (2)
- Predicates its devices cite: 3 (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
- Thermigen, Inc.: 1 (https://510kreport.com/company/thermigen)
- Hironic Co., Ltd.: 1 (https://510kreport.com/company/hironic)
- ShenB Co., Ltd.: 1 (https://510kreport.com/company/shenb)

## Recent decisions
- K233120: CWM-930S, Fixer DV9 (May 23, 2024)
- K222709: Retraction, CWM-910T, APOLEX Tite (Mar 21, 2023)

Source page: https://510kreport.com/company/chungwoo