FDA Device Establishments · JSON-LD · Markdown
FEI 3012392319 · Export Device to the United States But Perform No Other Operation on Device · Status: Active
| FEI Number | 3012392319 |
|---|---|
| Owner / Operator | ZIMMER, INC. (#1822565) |
| Address | 2323 Argentia Road, Mississauga Ontario, L5N 5N3, CA |
| Mandatory US Agent | Zimmer Biomet |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 2 |
| Product codes (top 20) | LPH, JDI |
| Regulation § (21 CFR) | 888.3358, 888.3350 |
| Proprietary names | LATERALIZED INTERGRAL POROUS PRIMARY FEMORAL COMPONENT |
Source: openFDA. Public-domain (CC0).