FDA Device Establishments · JSON-LD · Markdown
FEI 3004632523 · Repack or Relabel Medical Device Export Device to the United States But Perform No Other Operation on Device Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 3004632523 |
|---|---|
| Owner / Operator | Benestar Corp (#10039279) |
| Address | Baeckerstrasse 4-8, Luebbecke North Rhine-Westphalia, 32312, DE |
| Mandatory US Agent | Benestar Corp |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | FMP |
| Regulation § (21 CFR) | 880.6450 |
| Proprietary names | Toe Cap G, Medium 3 pieces; Corn Protection Plaster; Metatarsal Cushion G, 1 pair, polymer/fabric; Bunion Pad; Toe Divider GD Medium 3 pieces; Toe Rings; Blister Plaster 6 pieces; Hammer Toe pad G, Right, 1 piece; Metatarsal Cushion G, Polymer gel pads, 1 pair; Protective Plaster ¿ Thick, 4 pieces |
Source: openFDA. Public-domain (CC0).