FDA Device Establishments · JSON-LD · Markdown
FEI 2080783 · Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device · Status: Active
| FEI Number | 2080783 |
|---|---|
| Owner / Operator | NIHON KOHDEN CORP. (#8030227) |
| Address | 15353 Barranca Pkwy, Irvine, CA, US |
| Registration expiry | 2026 |
| Initial importer flag | Y |
| Registered products | 2 |
| Product codes (top 20) | GWQ, OLV |
| Regulation § (21 CFR) | 882.1400 |
| Proprietary names | TL-220T; TG-921T3; TL-052S; TL-201T; JE-921A; TL-062S |
Source: openFDA. Public-domain (CC0).