FDA Device Establishments · JSON-LD · Markdown
FEI 3010339638 · Remanufacture Medical Device · Status: Active
| FEI Number | 3010339638 |
|---|---|
| Owner / Operator | Devicor Medical Products, Inc. (#10033297) |
| Address | 4750 Lake Forest Dr Ste 120, Blue Ash, OH, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | NEU |
| Regulation § (21 CFR) | 878.4300 |
| Proprietary names | LumiMARK Biopsy Site Marker |
Source: openFDA. Public-domain (CC0).