FDA Device Establishments · JSON-LD · Markdown
FEI 3031284747 · Complaint File Establishment per 21 CFR 820.198 Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 3031284747 |
|---|---|
| Owner / Operator | Retropsoas Technologies, LLC (#10090791) |
| Address | 34 Countryside Lane, Frontenac, MO, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | LXH |
| Regulation § (21 CFR) | 888.4540 |
| Proprietary names | EARP Preparation and Insertion Instruments |
Source: openFDA. Public-domain (CC0).