FDA Device Establishments · JSON-LD · Markdown
FEI 3015537315 · Develop Specifications But Do Not Manufacture At This Facility Reprocess Single-Use Device Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device · Status: Active
| FEI Number | 3015537315 |
|---|---|
| Owner / Operator | CLARIPI Inc. (#10060777) |
| Address | 11 Ihwajang 1-gil, Jongro-gu, Seoul, 03100, KR |
| Mandatory US Agent | ClariPi USA Inc. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | LLZ |
| Regulation § (21 CFR) | 892.2050 |
| Proprietary names | ClariCT.AI |
Source: openFDA. Public-domain (CC0).