FDA Device Establishments · JSON-LD · Markdown
FEI 3007417776 · Manufacture Medical Device for Another Party (Contract Manufacturer) Manufacture Medical Device · Status: Active
| FEI Number | 3007417776 |
|---|---|
| Owner / Operator | T&L CO., LTD. (#9063857) |
| Address | 70-17, WONAM-RO, WONGOK-MYEON, ANSEONG-CITY Gyeonggi, 17554, KR |
| Mandatory US Agent | MEDIRECH GROUP LLC |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | NAD |
| Regulation § (21 CFR) | 878.4020 |
| Proprietary names | RenoFix NH; RenoCare Soft; RenoFix F; RenoFix N Nonwoven Plaster; RenoCare Hydrocolloid Dressing; RenoFix U roll Plaster; Suprasorb H; RenoFix MB Nonwoven Plaster; RenoCare B; RenoFix H |
Source: openFDA. Public-domain (CC0).