FDA Device Establishments · JSON-LD · Markdown
FEI 1045834 · Complaint File Establishment per 21 CFR 820.198 Repack or Relabel Medical Device Manufacture Medical Device · Status: Active
| FEI Number | 1045834 |
|---|---|
| Owner / Operator | THE ANSPACH EFFORT, INC. (#1045834) |
| Address | 4500 RIVERSIDE DR., Palm Bch Gdns, FL, US |
| Registration expiry | 2026 |
| Initial importer flag | Y |
| Registered products | 2 |
| Product codes (top 20) | DZI, DZJ |
| Regulation § (21 CFR) | 872.4120 |
| Proprietary names | Synthes |
Source: openFDA. Public-domain (CC0).