FDA Device Establishments · JSON-LD · Markdown
FEI 3008178161 · Manufacture Medical Device for Another Party (Contract Manufacturer) · Status: Active
| FEI Number | 3008178161 |
|---|---|
| Owner / Operator | KAINOS LABORATORIES INC (#10030967) |
| Address | 3-5 Aza Yarokuuchi Inada, Kasama Ibaraki, 309-1635, JP |
| Mandatory US Agent | Emergo Global Representation LLC |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | LCP |
| Regulation § (21 CFR) | 864.7470 |
| Proprietary names | Lucica Glycated Albumin-L |
Source: openFDA. Public-domain (CC0).