FDA Device Establishments · JSON-LD · Markdown
FEI 3015212522 · Manufacture Medical Device · Status: Active
| FEI Number | 3015212522 |
|---|---|
| Owner / Operator | WETAPE, Inc. (#10090089) |
| Address | 318 Jinwi-ro, Jinwi-myun, Pyeongtaek Gyeonggi, 17711, KR |
| Mandatory US Agent | Implus Footcare, LLC |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | KGX |
| Regulation § (21 CFR) | 880.5240 |
Source: openFDA. Public-domain (CC0).