FDA Device Establishments · JSON-LD · Markdown
FEI 3015550326 · Develop Specifications But Do Not Manufacture At This Facility Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device · Status: Active
| FEI Number | 3015550326 |
|---|---|
| Owner / Operator | TrueRelief (#10060510) |
| Address | 100 Wilshire Boulevard, Suite 700, Santa Monica, CA, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | GZJ |
| Regulation § (21 CFR) | 882.5890 |
| Proprietary names | TRUERELIEF, Model 1250 TRUERELIEF Device, TRUERELIEF 1250; TRUERELIEF Secondary Probe, Model P12S Secondary Probe; TRUERELIEF Probe Tips, Probe Tips, Model P12T10 Probe Tips; TRUERELIEF Primary Probe, Model P12P Primary Probe; TRUERELIEF Kit, Model TR1250C TRUERELIEF Kit; TRUERELIEF Power Cord with Wall Wart, Model WW12 Power Cord with Wall Wart |
Source: openFDA. Public-domain (CC0).