FDA Device Establishments · JSON-LD · Markdown
FEI 3015259874 · Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 3015259874 |
|---|---|
| Owner / Operator | Pellecome LLC (#10059229) |
| Address | 240 Main Street, Bldg A, Suite 1, Gladstone, NJ, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | GDX |
| Regulation § (21 CFR) | 878.4800 |
| Proprietary names | Re3 Male Scalpel |
Source: openFDA. Public-domain (CC0).