FDA Device Establishments · JSON-LD · Markdown
FEI 3015417614 · Develop Specifications But Do Not Manufacture At This Facility Complaint File Establishment per 21 CFR 820.198 · Status: Active
| FEI Number | 3015417614 |
|---|---|
| Owner / Operator | Rinovum Subsidiary 2, LLC (#10060129) |
| Address | 4923 Simmons Circle, Export, PA, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | HHW |
| Regulation § (21 CFR) | 884.3575 |
| Proprietary names | Revive |
Source: openFDA. Public-domain (CC0).