FDA Device Establishments · JSON-LD · Markdown
FEI 3006254866 · Repack or Relabel Medical Device Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device · Status: Active
| FEI Number | 3006254866 |
|---|---|
| Owner / Operator | ActiGraph, LLC (#10023162) |
| Address | 70 North Baylen Street, Suite 400, Pensacola, FL, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 5 |
| Product codes (top 20) | DQA, MWI, MSX, DRG, BZQ |
| Regulation § (21 CFR) | 870.2700, 870.2300, 870.2910, 868.2375 |
| Proprietary names | Everion+ (G2) System |
Source: openFDA. Public-domain (CC0).