FDA Device Establishments · JSON-LD · Markdown
FEI 1000136003 · Manufacture Medical Device for Another Party (Contract Manufacturer) Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device · Status: Active
| FEI Number | 1000136003 |
|---|---|
| Owner / Operator | Greenwood Marketing LLC (#10050483) |
| Address | 332 E BROADWAY, BRANDENBURG, KY, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | ITW |
| Regulation § (21 CFR) | 890.3475 |
| Proprietary names | NeuroFlex Restorative Flex Boot; RM Pediatric Safe Boot; Flo-Form Complete Care Boot; RM Safe Boot II; RM Safe Boot I; SUN TAFO - Flo-Form Fluidized Boot; Dynamic Control Boot; NeuroFlex Restorative FootEase; Flo-Form RM Fluidized Boot; Complete CAIR Boot |
Source: openFDA. Public-domain (CC0).