FDA Device Establishments · JSON-LD · Markdown
FEI 3030861184 · Manufacture Medical Device Complaint File Establishment per 21 CFR 820.198 · Status: Active
| FEI Number | 3030861184 |
|---|---|
| Owner / Operator | Tullo, LLC (#10090290) |
| Address | 22701 Hall Rd Ste 100, Macomb, MI, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | GAD |
| Regulation § (21 CFR) | 878.4800 |
| Proprietary names | Facilitator Posterior Glenoid Retractor, Facilitator-Standard; Shoulder-Side Entry Glenosphere Inserter, SEGI-3338; Facilitator Posterior Glenoid Retractor, Facilitator-Small; Shoulder-Side Entry Glenosphere Inserter, SEGI-3944 |
Source: openFDA. Public-domain (CC0).