FDA Device Establishments · JSON-LD · Markdown
FEI 3005801723 · Complaint File Establishment per 21 CFR 820.198 Develop Specifications But Do Not Manufacture At This Facility Export Device to the United States But Perform No Other Operation on Device Manufacture Medical Device · Status: Active
| FEI Number | 3005801723 |
|---|---|
| Owner / Operator | LIGHT INSTRUMENTS Ltd. (#9089640) |
| Address | 4 Hatnufa Street, Yokneam, Yokneam Northern, 2066717, IL |
| Mandatory US Agent | Sterling Medical Devices, LLC DBA Vantage MedTech |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | GEX |
| Regulation § (21 CFR) | 878.4810 |
| Proprietary names | D-STORM |
Source: openFDA. Public-domain (CC0).