FDA Device Establishments · JSON-LD · Markdown
FEI 3012470925 · Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device · Status: Active
| FEI Number | 3012470925 |
|---|---|
| Owner / Operator | XTREEM PULSE (#10057865) |
| Address | 690 Washington St, # 4B, New York, NY, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | NFO |
| Regulation § (21 CFR) | 882.5890 |
| Proprietary names | PureLift Pro Plus |
Source: openFDA. Public-domain (CC0).