FDA Device Establishments · JSON-LD · Markdown
FEI 1000123280 · Manufacture Medical Device Repack or Relabel Medical Device · Status: Active
| FEI Number | 1000123280 |
|---|---|
| Owner / Operator | Kerma Medical Products, Inc. (#9004008) |
| Address | 215 Suburban Dr, Suffolk, VA, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | ISR |
| Regulation § (21 CFR) | 890.3025 |
| Proprietary names | FMB |
Source: openFDA. Public-domain (CC0).