# KEGO CORPORATION

FEI: 3008603863
Status: Active
Establishment types: Export Device to the United States But Perform No Other Operation on Device
Owner/operator: KEGO Corporation (#10052258)

Address: 4350 Castleton Rd., Unit 3-4, London Ontario, N6N 0A3, CA

Mandatory US Agent: FDAbasics

## Products

Total registered: 1
Top product codes: ILT
Regulation §: 890.5050

Proprietary names: ADAPTOR, RECREATIONAL, MULTIPLE TYPES

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223008603863%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3008603863