FDA Device Establishments · JSON-LD · Markdown
FEI 3001415984 · Manufacture Medical Device Remanufacture Medical Device Complaint File Establishment per 21 CFR 820.198 · Status: Active
| FEI Number | 3001415984 |
|---|---|
| Owner / Operator | SCITON, INC. (#9033367) |
| Address | 925 COMMERCIAL STREET, Palo Alto, CA, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | GEX |
| Regulation § (21 CFR) | 878.4810 |
| Proprietary names | mJoule |
Source: openFDA. Public-domain (CC0).