FDA Device Establishments · JSON-LD · Markdown
FEI 3019543072 · Repack or Relabel Medical Device · Status: Active
| FEI Number | 3019543072 |
|---|---|
| Owner / Operator | HYDROFERA, LLC. (#9028346) |
| Address | 8 Progress Drive, --, Manchester, CT, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | GDY |
| Regulation § (21 CFR) | 878.4450 |
| Proprietary names | Keel Sponge |
Source: openFDA. Public-domain (CC0).