FDA Device Establishments · JSON-LD · Markdown
FEI 3021841055 · Repack or Relabel Medical Device · Status: Active
| FEI Number | 3021841055 |
|---|---|
| Owner / Operator | MERET USA LLC (#10084520) |
| Address | 151 SHIPYARD WAY, SUITE B, Newport Beach, CA, US |
| Registration expiry | 2026 |
| Initial importer flag | Y |
| Registered products | 1 |
| Product codes (top 20) | KGX |
| Regulation § (21 CFR) | 880.5240 |
| Proprietary names | MERET |
Source: openFDA. Public-domain (CC0).