FDA Device Establishments · JSON-LD · Markdown
FEI 3012818008 · Repack or Relabel Medical Device · Status: Active
| FEI Number | 3012818008 |
|---|---|
| Owner / Operator | PureTek Corporation (#10052870) |
| Address | 7900 NELSON RD STE A, Panorama City, CA, US |
| Registration expiry | 2026 |
| Initial importer flag | Y |
| Registered products | 1 |
| Product codes (top 20) | MDA |
| Regulation § (21 CFR) | 878.4025 |
| Proprietary names | Silicon Sheet |
Source: openFDA. Public-domain (CC0).