FDA Device Establishments · JSON-LD · Markdown
FEI 3002754162 · Manufacture Medical Device for Another Party (Contract Manufacturer) Repack or Relabel Medical Device · Status: Active
| FEI Number | 3002754162 |
|---|---|
| Owner / Operator | PURE SOURCE, LLC (#10047786) |
| Address | 9750 NW 17th St, Doral, FL, US |
| Registration expiry | 2026 |
| Initial importer flag | Y |
| Registered products | 1 |
| Product codes (top 20) | MDA |
| Regulation § (21 CFR) | 878.4025 |
| Proprietary names | Scarcin Gel; Scarcin Roll On |
Source: openFDA. Public-domain (CC0).