# Flint Rehabilitation Devices, LLC

FEI: 3010664759
Status: Active
Establishment types: Complaint File Establishment per 21 CFR 820.198; Manufacture Medical Device
Owner/operator: Flint Rehabilitation Devices, LLC (#10045919)

Address: 18023 SKY PARK CIR STE H2, Irvine, CA, US



## Products

Total registered: 1
Top product codes: KNO
Regulation §: 890.3910

Proprietary names: Boost Arm Support

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223010664759%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3010664759