# DFI CO., LTD.

FEI: 3005841640
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: DFI CO., LTD. (#9089171)

Address: 388-25 Gomo-Ro, Jillye-Myeon, Gimhae Jeonnam, 50875, KR

Mandatory US Agent: LK Consulting Group USA, Inc.

## Products

Total registered: 10
Top product codes: JIN, LJX, JMA, CEN, CDM, JIL, JIR, JIO, JMT, JJB
Regulation §: 862.1435, 864.7675, 862.1095, 862.1550, 862.1785, 862.1340, 862.1645, 864.6550, 862.1510, 862.1115

Proprietary names: QTEST™ 11, CYBOW 10

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223005841640%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3005841640