FDA Device Establishments · JSON-LD · Markdown
FEI 3012336461 · Complaint File Establishment per 21 CFR 820.198 Repack or Relabel Medical Device Manufacture Medical Device · Status: Active
| FEI Number | 3012336461 |
|---|---|
| Owner / Operator | The Linden Group Corp. (#9092461) |
| Address | 2B Wing Dr, Cedar Knolls, NJ, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | KQM |
| Regulation § (21 CFR) | 878.4160 |
| Proprietary names | Optik View SC2784XX Series; Optik View SC551X; Optik View SC3184XX Series; 42" Vividimage W HD Wall Display; Optik View SC6584XX Series; Optik View SC242XX; Optik View SC5584XX Series; Optik View SC421X; Optik View SC191XX; SC4284XX Series |
Source: openFDA. Public-domain (CC0).