FDA Device Establishments · JSON-LD · Markdown
FEI 3007350713 · Complaint File Establishment per 21 CFR 820.198 Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device · Status: Active
| FEI Number | 3007350713 |
|---|---|
| Owner / Operator | Quality Electrodynamics (#10023379) |
| Address | 6655 Beta Drive Suite 100, Mayfield Village, OH, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | MOS |
| Regulation § (21 CFR) | 892.1000 |
| Proprietary names | 8ch Knee SPEEDER |
Source: openFDA. Public-domain (CC0).