FDA Device Establishments · JSON-LD · Markdown
FEI 3012696653 · Complaint File Establishment per 21 CFR 820.198 Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 3012696653 |
|---|---|
| Owner / Operator | VentureMed Group, Inc. (#10052004) |
| Address | 2800 Campus Dr., Suite 50, Plymouth, MN, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | PNO |
| Regulation § (21 CFR) | 870.1250 |
| Proprietary names | FLEX Vessel Prep System |
Source: openFDA. Public-domain (CC0).