FDA Device Establishments · JSON-LD · Markdown
FEI 3005516815 · Repack or Relabel Medical Device · Status: Active
| FEI Number | 3005516815 |
|---|---|
| Owner / Operator | MYKITA North America (#10044968) |
| Address | 80 Main St Ste 200, West Orange, NJ, US |
| Registration expiry | 2026 |
| Initial importer flag | Y |
| Registered products | 1 |
| Product codes (top 20) | HQZ |
| Regulation § (21 CFR) | 886.5842 |
| Proprietary names | MYKITA MYLON; MYKITA; MYKITA Lite; MYKITA Col No.1; MYKITA Col No.2 |
Source: openFDA. Public-domain (CC0).