FDA Device Establishments · JSON-LD · Markdown
FEI 3013696225 · Manufacture Medical Device · Status: Active
| FEI Number | 3013696225 |
|---|---|
| Owner / Operator | Kurin, Inc. (#10057862) |
| Address | 10840 Thornmint Road, Suite 111, San Diego, CA, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 2 |
| Product codes (top 20) | JKA, FPA |
| Regulation § (21 CFR) | 862.1675, 880.5440 |
| Proprietary names | Product Codes with Jet Lock Technology (without extension set) - DJ-PIV12, MJ-PIV12, TJ-PIV12, SJ-PIV4; Product Codes with Kurin Lock Technology (with extension set) - D-PIV18, M-PIV18, T-PIV18, S-PIV10; Product Codes w/Kurin Lock Technology (Venipuncture, Slide) - D-11221, D-11223, M-11221, M-11223, T-11221, T-11223; Product Codes w/Jet Lock Technology (Venipuncture, Slide) - DJ-121, D-123, M-121, M-123, T-121, T-123; Product Codes w/Kurin Lock Technology (Venipuncture, Push-Button) - D-21221, D-21223, M-21221, M-21223, T-21221, T-21223; Product Codes with Kurin Lock Technology (without extension set) - D-PIV12, M-PIV12, T-PIV12, S-PIV4; Product Codes w/Jet Lock Technology (Venipuncture, Push-Button) - DJ-221, D-223, M-221, M-223, T-221, T-223; Product Codes with Jet Lock Technology (with extension set) - DJ-PIV18, MJ-PIV18, TJ-PIV18, SJ-PIV10 |
Source: openFDA. Public-domain (CC0).