FDA Device Establishments · JSON-LD · Markdown
FEI 3009134882 · Manufacture Medical Device · Status: Active
| FEI Number | 3009134882 |
|---|---|
| Owner / Operator | Dmed (#10037526) |
| Address | Innovation Tower, 111, Sagimakgol-ro, Jungwon-gu, Seongnam-si Gyeonggi, 13202, KR |
| Mandatory US Agent | K resource Corp |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | GDF |
| Regulation § (21 CFR) | 878.4800 |
| Proprietary names | Curve; Helix; Mini Sling Guide |
Source: openFDA. Public-domain (CC0).