FDA Device Establishments · JSON-LD · Markdown
FEI 3012669304 · Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 3012669304 |
|---|---|
| Owner / Operator | Prevent-Plus, LLC (#10052036) |
| Address | 4220 Duncan Ave, Suite 201, Saint Louis, MO, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | KMF |
| Regulation § (21 CFR) | 880.5090 |
| Proprietary names | Preventogen |
Source: openFDA. Public-domain (CC0).