FDA Device Establishments · JSON-LD · Markdown
FEI 1526350 · Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device · Status: Active
| FEI Number | 1526350 |
|---|---|
| Owner / Operator | ZIMMER, INC. (#1822565) |
| Address | 200 WEST OHIO AVE., Dover, OH, US |
| Registration expiry | 2026 |
| Initial importer flag | Y |
| Registered products | 1 |
| Product codes (top 20) | GFA |
| Regulation § (21 CFR) | 878.4820 |
| Proprietary names | Raps; Procedure Pack; Keels; OSCILLATING SAW BLADE; STABLECUT; RECIPROCATING SAW BLADE |
Source: openFDA. Public-domain (CC0).