FDA Device Establishments · JSON-LD · Markdown
FEI 3003917473 · Repack or Relabel Medical Device Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device · Status: Active
| FEI Number | 3003917473 |
|---|---|
| Owner / Operator | ANODIA SYSTEMS, LLC (#9053125) |
| Address | 109 LARRIMORE LANE, Danville, KY, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | EIA |
| Regulation § (21 CFR) | 872.6640 |
| Proprietary names | C-1805M; MAK-1805; DentaKLEEN; VELOCITY WATER; PRO-KLEEN; MAK-1910 |
Source: openFDA. Public-domain (CC0).