# LUMINOAH

FEI: 3046434077
Status: Active
Establishment types: Complaint File Establishment per 21 CFR 820.198; Develop Specifications But Do Not Manufacture At This Facility; Manufacture Medical Device
Owner/operator: Luminoah (#10096019)

Address: 1 Morton Dr Ste 100, Charlottesville, VA, US



## Products

Total registered: 1
Top product codes: LZH
Regulation §: 880.5725

Proprietary names: Luminoah Flow Enteral Nutrition Delivery System, Luminoah Flow Enteral Pump, Luminoah Flow Enteral System, Luminoah Flow Enteral Feeding Pump, Luminoah Flow Enteral Nutrition System

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223046434077%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3046434077