FDA Device Establishments · JSON-LD · Markdown
FEI 3031563240 · Complaint File Establishment per 21 CFR 820.198 Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 3031563240 |
|---|---|
| Owner / Operator | GRASP AS (#10091002) |
| Address | Oyro 55, OS Hordaland, 5200, NO |
| Mandatory US Agent | CENIT Consulting |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | ILQ |
| Regulation § (21 CFR) | 890.3710 |
| Proprietary names | Grasp Aware; Grasp Device |
Source: openFDA. Public-domain (CC0).