FDA Device Establishments · JSON-LD · Markdown
FEI 3007134923 · Repack or Relabel Medical Device Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 3007134923 |
|---|---|
| Owner / Operator | ProMedTek, Inc. (#10026515) |
| Address | 15475 N Greenway Hayden Loop Ste 21-22b, Scottsdale, AZ, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | IMJ |
| Regulation § (21 CFR) | 890.5290 |
| Proprietary names | Replexa+ |
Source: openFDA. Public-domain (CC0).