FDA Device Establishments · JSON-LD · Markdown
FEI 3018188770 · Repack or Relabel Medical Device Export Device to the United States But Perform No Other Operation on Device Complaint File Establishment per 21 CFR 820.198 · Status: Active
| FEI Number | 3018188770 |
|---|---|
| Owner / Operator | Lustre Skin Ltd (#10080478) |
| Address | Alba Innovation Centre, Alba Campus, Livingston Scotland, EH54 7GA, GB |
| Mandatory US Agent | Smith Associates |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 3 |
| Product codes (top 20) | OHS, ILY, OLP |
| Regulation § (21 CFR) | 878.4810, 890.5500 |
| Proprietary names | LUSTRE ClearSkin REVIVE LED Light Therapy Mask |
Source: openFDA. Public-domain (CC0).