FDA Device Establishments · JSON-LD · Markdown
FEI 2244812 · Repack or Relabel Medical Device · Status: Active
| FEI Number | 2244812 |
|---|---|
| Owner / Operator | DMG America, L.L.C. (#2244812) |
| Address | 242 S Dean St, ENGLEWOOD, NJ, US |
| Registration expiry | 2026 |
| Initial importer flag | Y |
| Registered products | 1 |
| Product codes (top 20) | LBH |
| Regulation § (21 CFR) | 872.3260 |
| Proprietary names | Varnish, Cavity - Kolorz |
Source: openFDA. Public-domain (CC0).