FDA Device Establishments · JSON-LD · Markdown
FEI 3027262786 · Repack or Relabel Medical Device · Status: Active
| FEI Number | 3027262786 |
|---|---|
| Owner / Operator | Solendos., INC. (#10089428) |
| Address | #503 5F, E&C VENTURE DREAM TOWER3 38-21 DIGITAL-RO 31 GIL,, GURO-GU, SEOUL, GURO-GU Seoul, 08376, KR |
| Mandatory US Agent | Cori Ragan |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | FZS |
| Regulation § (21 CFR) | 878.4800 |
| Proprietary names | [Target] TCU0005 Reverse Curette 3mm; [Target] TCU0004 Bone Curette 6mm Wang; [Target] TCU0006 Boomerang Curette 3mm; [Target] TCU0003 Bone Curette 5mm Maximus; [Target] TCU0002 Bone Curette 3mm Bishop |
Source: openFDA. Public-domain (CC0).