FDA Device Establishments · JSON-LD · Markdown
FEI 3010551934 · Manufacture Medical Device · Status: Active
| FEI Number | 3010551934 |
|---|---|
| Owner / Operator | SAEYANG CO., LTD. (#10086948) |
| Address | (Galsan-Dong), 348 SEONGSEO-RO, DALSEO-GU Daegu, 42697, KR |
| Mandatory US Agent | KMC USA, Inc |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | EKX |
| Regulation § (21 CFR) | 872.4200 |
| Proprietary names | Endo A Class; CanalPro CL2 |
Source: openFDA. Public-domain (CC0).