FDA Device Establishments · JSON-LD · Markdown
FEI 3031294900 · Manufacture Medical Device · Status: Active
| FEI Number | 3031294900 |
|---|---|
| Owner / Operator | Okapi Medical dba Resivant Medical (#10092381) |
| Address | 526 S Main St # 124m, Akron, OH, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 2 |
| Product codes (top 20) | MPN, OMD |
| Regulation § (21 CFR) | 878.4010, 878.4011 |
| Proprietary names | CUTIVA(TM) PLUS Skin Closure System (RM-1739) |
Source: openFDA. Public-domain (CC0).