FDA Device Establishments · JSON-LD · Markdown
FEI 3042158718 · Complaint File Establishment per 21 CFR 820.198 Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device for Another Party (Contract Manufacturer) · Status: Active
| FEI Number | 3042158718 |
|---|---|
| Owner / Operator | OpenPatch Inc. (#10094030) |
| Address | 11 F.-1, No. 24, Sec. 4, Xinyi Rd., Da'an Dist., Taipei, 106, TW |
| Mandatory US Agent | Willow Glen Consultancy LLC |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | KOY |
| Regulation § (21 CFR) | 878.4730 |
| Proprietary names | OpenPatch Super Vi Sting Free Adhesive Remover (Non-Sterile) |
Source: openFDA. Public-domain (CC0).