# DFI Co., Ltd.

- Location (FDA's records): Gyeongsangnam-Do, KR
- FDA decisions: 4 (2006–2018): 4 510(k) clearances
- Product codes: JIL (3), KQO (1)
- 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
- Siemens Healthcare Diagnostics, Inc.: 1 (https://510kreport.com/company/siemens-healthcare-diagnostics)
- Heraeus Kulzer, Inc.: 1 (https://510kreport.com/company/heraeus-kulzer)
- Bayer Corp.: 1 (https://510kreport.com/company/bayer)

## Recent decisions
- K181024: DUS 2GP Reagent Strips, DUS 5 Reagent Strips, DUS 10 Reagent Strips (May 23, 2018)
- K171521: DUS R-50S (Urine Chemistry system) (Feb 16, 2018)
- K102188: Cybow Reader, Models 300 & 720 (Aug 9, 2011)
- K052525: Cybow 11 Series Reagent Strips for Urinalysis (Mar 29, 2006)

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