FDA Device Establishments · JSON-LD · Markdown

AURORA DERMO CORP

FEI 3039935725 · Repack or Relabel Medical Device · Status: Active

FEI Number3039935725
Owner / OperatorAURORA DERMO CORP (#10096096)
Address6303 Waterford District Dr Ste 400, Miami, FL, US
Registration expiry2026
Initial importer flagY
Registered products2
Product codes (top 20)GEX, ONF
Regulation § (21 CFR)878.4810
Proprietary namesLUMINA

External sources

Source: openFDA. Public-domain (CC0).