FDA Device Establishments · JSON-LD · Markdown
FEI 3022764539 · Manufacture Medical Device · Status: Active
| FEI Number | 3022764539 |
|---|---|
| Owner / Operator | LUCA AICell (#10085130) |
| Address | 3rd floor, 11-35, Simin-daero 327beon-gil, Dongan-gu, Anyang-si Gyeonggi, 14055, KR |
| Mandatory US Agent | KMC USA, Inc |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | NEC |
| Regulation § (21 CFR) | 880.5090 |
| Proprietary names | SKINTACT (Model: MD01-01D) |
Source: openFDA. Public-domain (CC0).