FDA Device Establishments · JSON-LD · Markdown
FEI 3007602302 · Repack or Relabel Medical Device · Status: Active
| FEI Number | 3007602302 |
|---|---|
| Owner / Operator | Danmic Global, LLC (#10029364) |
| Address | 2059 CAMDEN AVE # 281, SAN JOSE, CA, US |
| Registration expiry | 2026 |
| Initial importer flag | Y |
| Registered products | 1 |
| Product codes (top 20) | GXB |
| Regulation § (21 CFR) | 882.1500 |
| Proprietary names | AESTHESIO |
Source: openFDA. Public-domain (CC0).