FDA Device Establishments · JSON-LD · Markdown
FEI 3010050274 · Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device · Status: Active
| FEI Number | 3010050274 |
|---|---|
| Owner / Operator | Regenerative Technologies Corp dba Juvent (#10042771) |
| Address | 9420 Ooltewah Industrial Road, Suite 1, Ooltewah, TN, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | BXB |
| Regulation § (21 CFR) | 890.5380 |
| Proprietary names | Juvent 1000 |
Source: openFDA. Public-domain (CC0).