FDA Device Establishments · JSON-LD · Markdown
FEI 3016247852 · Develop Specifications But Do Not Manufacture At This Facility Complaint File Establishment per 21 CFR 820.198 · Status: Active
| FEI Number | 3016247852 |
|---|---|
| Owner / Operator | Avanti (#10062225) |
| Address | 1245 Hollow Road, Penn Valley, PA, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 2 |
| Product codes (top 20) | HWC, HRS |
| Regulation § (21 CFR) | 888.3040, 888.3030 |
| Proprietary names | Avanti Ulnar Plates; Avanti Wrist Spanning Plates; Avanti Forearm Plates; Avanti Cannulated Screw; Avanti Distal Radius Plates; Avanti Wrist Fusion Plates |
Source: openFDA. Public-domain (CC0).