FDA Device Establishments · JSON-LD · Markdown
FEI 3017278832 · Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device · Status: Active
| FEI Number | 3017278832 |
|---|---|
| Owner / Operator | Bend It Technologies LTD. (#10077053) |
| Address | 25 Basel Street, Petach Tikva Central, 4951038, IL |
| Mandatory US Agent | Heyer Regulatory Solutions LLC |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 2 |
| Product codes (top 20) | DQY, QJP |
| Regulation § (21 CFR) | 870.1250 |
| Proprietary names | Bendit17 Microcatheter |
Source: openFDA. Public-domain (CC0).