FDA Device Establishments · JSON-LD · Markdown
FEI 3011489618 · Manufacture Medical Device · Status: Active
| FEI Number | 3011489618 |
|---|---|
| Owner / Operator | TAEYEON MEDICAL Co., Ltd. (#10089805) |
| Address | 132-1 Donghwagongdan-Ro, Munmak-eup, Wonju-si Gangwon, 26365, KR |
| Mandatory US Agent | LK Consulting Group USA, Inc. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | NKB |
| Regulation § (21 CFR) | 888.3070 |
| Proprietary names | Dyflex-II |
Source: openFDA. Public-domain (CC0).