FDA Device Establishments · JSON-LD · Markdown
FEI 3007219818 · Manufacture Medical Device for Another Party (Contract Manufacturer) · Status: Active
| FEI Number | 3007219818 |
|---|---|
| Owner / Operator | Custom Converting, Inc. (#10085051) |
| Address | 2625 Temple Heights Dr., Suite C, Oceanside, CA, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | FMP |
| Regulation § (21 CFR) | 880.6450 |
| Proprietary names | Releef Direct Solutions Sore Feet Insole; Releef Direct Solutions Cracked Heel Insole; Releef Direct Solutions Circulation Insole |
Source: openFDA. Public-domain (CC0).