FDA Device Establishments · JSON-LD · Markdown
FEI 3033307563 · Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device · Status: Active
| FEI Number | 3033307563 |
|---|---|
| Owner / Operator | Rejoni, Inc (#10091756) |
| Address | 201 Burlington Rd, Bedford, MA, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | LKF |
| Regulation § (21 CFR) | 884.4530 |
| Proprietary names | Rejoni Acorn Catheter |
Source: openFDA. Public-domain (CC0).