# AURORA DERMO CORP

FEI: 3039935725
Status: Active
Establishment types: Repack or Relabel Medical Device
Owner/operator: AURORA DERMO CORP (#10096096)

Address: 6303 Waterford District Dr Ste 400, Miami, FL, US



## Products

Total registered: 2
Top product codes: GEX, ONF
Regulation §: 878.4810

Proprietary names: LUMINA

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223039935725%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3039935725