FDA Device Establishments · JSON-LD · Markdown
FEI 1718791 · Manufacture Medical Device · Status: Active
| FEI Number | 1718791 |
|---|---|
| Owner / Operator | D.O. WEAVER AND COMPANY (#1718791) |
| Address | 565 NUCLA WAY, UNIT B, Aurora, CO, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | DRX |
| Regulation § (21 CFR) | 870.2360 |
| Proprietary names | Nuprep Skin Prep Gel |
Source: openFDA. Public-domain (CC0).