# Idis Co., Ltd.

- Location (FDA's records): Bucheon-Si, KR
- FDA decisions: 1 (2023–2023): 1 510(k) clearance
- Product codes: DZE (1)
- Predicates its devices cite: 4 (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
- Dio Corporation: 1 (https://510kreport.com/company/dio)
- Dentium Co., Ltd.: 1 (https://510kreport.com/company/dentium)
- Osstem Implant Co., Ltd.: 1 (https://510kreport.com/company/osstem-implant)
- Hiossen, Inc.: 1 (https://510kreport.com/company/hiossen)

## Recent decisions
- K231429: S-Plant Dental Implant System (Dec 18, 2023)

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