FDA Device Establishments · JSON-LD · Markdown
FEI 3006793151 · Repack or Relabel Medical Device · Status: Active
| FEI Number | 3006793151 |
|---|---|
| Owner / Operator | Gurin Products, LLC (#10031258) |
| Address | 2522 Chambers Rd Ste 100, Tustin, CA, US |
| Registration expiry | 2026 |
| Initial importer flag | Y |
| Registered products | 1 |
| Product codes (top 20) | DXQ |
| Regulation § (21 CFR) | 870.1120 |
| Proprietary names | SP-110ND; SPR-210B; SPR-210P; SPS-120 |
Source: openFDA. Public-domain (CC0).