FDA Device Establishments · JSON-LD · Markdown
FEI 3010143171 · Manufacture Medical Device for Another Party (Contract Manufacturer) · Status: Active
| FEI Number | 3010143171 |
|---|---|
| Owner / Operator | AR Fabricating (#10043437) |
| Address | 40132 Industrial Park Cir Ste 102, Georgetown, TX, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | MAX |
| Regulation § (21 CFR) | 888.3080 |
| Proprietary names | PLIF Peek Implant; Lateral Peek Implant; TLIF Peek Implant; Cervical Peek Implant |
Source: openFDA. Public-domain (CC0).