FDA Device Establishments · JSON-LD · Markdown
FEI 3022978896 · Complaint File Establishment per 21 CFR 820.198 Repack or Relabel Medical Device Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 3022978896 |
|---|---|
| Owner / Operator | Bimini Health Tech (#10048045) |
| Address | 8400 Belleview Drive, Ste. 125, Plano, TX, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | QKL |
| Regulation § (21 CFR) | 878.5040 |
| Proprietary names | Puregraft 50 |
Source: openFDA. Public-domain (CC0).