FDA Device Establishments · JSON-LD · Markdown
FEI 3005841640 · Manufacture Medical Device · Status: Active
| FEI Number | 3005841640 |
|---|---|
| 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. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 10 |
| Product codes (top 20) | JIN, LJX, JMA, CEN, CDM, JIL, JIR, JIO, JMT, JJB |
| Regulation § (21 CFR) | 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. Public-domain (CC0).