# Daeju Meditech Engineering Co., Ltd.

- Location (FDA's records): Seoul, KR
- FDA decisions: 3 (2021–2025): 3 510(k) clearances
- Product codes: GEX (3)
- 510(k) review time since 2016: median 99 days, against 90 for FDA's reviews in the same codes and years (2 of 3 faster)
- 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
- Ilooda Co,., Ltd.: 1 (https://510kreport.com/company/ilooda)
- Laseroptek Co., Ltd.: 1 (https://510kreport.com/company/laseroptek)
- Hironic Co., Ltd.: 1 (https://510kreport.com/company/hironic)

## Recent decisions
- K242207: Noable Laser (Mar 7, 2025)
- K242206: Activo (Sep 27, 2024)
- K211637: Aroma Grand (Sep 3, 2021)

Source page: https://510kreport.com/company/daeju-meditech-engineering