FDA Device Establishments · JSON-LD · Markdown
FEI 3025032529 · Manufacture Medical Device Manufacture Medical Device for Another Party (Contract Manufacturer) · Status: Active
| FEI Number | 3025032529 |
|---|---|
| Owner / Operator | VIVATEC Co.,Ltd. (#10092839) |
| Address | 2-10-1,Kitahanada-cho,Kita-ku,, Sakai-shi Osaka, 591-8002, JP |
| Mandatory US Agent | Frederick Hart Co., Inc. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | EFW |
| Regulation § (21 CFR) | 872.6855 |
| Proprietary names | TOOTHBRUSH, MANUAL |
Source: openFDA. Public-domain (CC0).