FDA Device Establishments · JSON-LD · Markdown
FEI 3010621943 · Manufacture Medical Device for Another Party (Contract Manufacturer) Repack or Relabel Medical Device Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device · Status: Active
| FEI Number | 3010621943 |
|---|---|
| Owner / Operator | Corflex Global, LLC (#1218997) |
| Address | Zona Franca Industrial de San Isidro, antigua nave MFI-2, Santo Domingo Este, 15801, DO |
| Mandatory US Agent | Corflex |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | ITQ |
| Regulation § (21 CFR) | 890.3475 |
| Proprietary names | CKI STRAP 12"; CKI / WHEATON STRAP 8"; CKI/ WHEATON STRAP 12"; CKI / WHEATON STRAP 10"; CKI STRAP 10" |
Source: openFDA. Public-domain (CC0).