FDA Device Establishments · JSON-LD · Markdown
FEI 3038277270 · Complaint File Establishment per 21 CFR 820.198 Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 3038277270 |
|---|---|
| Owner / Operator | Byonyks Medical Devices Inc (#10093651) |
| Address | 550 E Devon Ave Ste 140, Itasca, IL, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 2 |
| Product codes (top 20) | FKX, KDJ |
| Regulation § (21 CFR) | 876.5630 |
| Proprietary names | Byonyks X-1 APD Cycler; Byonyks Automated PD Set DS-1 |
Source: openFDA. Public-domain (CC0).