FDA Device Establishments · JSON-LD · Markdown
FEI 3032847809 · Repack or Relabel Medical Device Manufacture Medical Device Remanufacture Medical Device · Status: Active
| FEI Number | 3032847809 |
|---|---|
| Owner / Operator | MEBSTER Inc. (#10091573) |
| Address | 101 W Dickman St, Baltimore, MD, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | IQI |
| Regulation § (21 CFR) | 890.3475 |
| Proprietary names | UNILEXA PRIME 2.1; UNILEXA HOME kit 2.1 |
Source: openFDA. Public-domain (CC0).