FDA Device Establishments · JSON-LD · Markdown
FEI 3015168749 · Manufacture Medical Device · Status: Active
| FEI Number | 3015168749 |
|---|---|
| Owner / Operator | MediThinQ Co., Ltd. (#10059499) |
| Address | 35 Pangyo-ro, 255beon-gil, Bundang-gu, Seongnam Gyeonggi, 13486, KR |
| Mandatory US Agent | LK Consulting Group USA, Inc. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | FEM |
| Regulation § (21 CFR) | 876.1500 |
| Proprietary names | SE-EDF; SE-RX3; GV-P1; GV-100; GV-CX2; SE-P1; GV-200C1; GV-200C2; ScopEYE Wired; GV-200 Main Unit |
Source: openFDA. Public-domain (CC0).