FDA Device Establishments · JSON-LD · Markdown
FEI 3003829667 · Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device · Status: Active
| FEI Number | 3003829667 |
|---|---|
| Owner / Operator | PLUSOPTIX GMBH (#9050572) |
| Address | Nordostpark 21, Nuremberg Bavaria, 90411, DE |
| Mandatory US Agent | Plusoptix Inc. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | HKO |
| Regulation § (21 CFR) | 886.1760 |
| Proprietary names | plusoptiX S20; plusoptiX A12; PowerRef 3; plusoptiX PR3; plusoptiX S16; plusoptiX A16; plusoptiX S12; plusoptiX A20 |
Source: openFDA. Public-domain (CC0).