FDA Device Establishments · JSON-LD · Markdown
FEI 3000210901 · Manufacture Medical Device · Status: Active
| FEI Number | 3000210901 |
|---|---|
| Owner / Operator | WOODWAY USA, INC. (#9026547) |
| Address | W234n700 Busse Rd, Vernon, WI, US |
| Registration expiry | 2026 |
| Initial importer flag | Y |
| Registered products | 1 |
| Product codes (top 20) | IOL |
| Regulation § (21 CFR) | 890.5380 |
| Proprietary names | PPS 43; PPS 70; PPS 55; Continuum; 4Front Med; Boost 2; Pro Med; Pro XL Med |
Source: openFDA. Public-domain (CC0).