# STOMATOTECH

FEI: 3010966817
Status: Active
Establishment types: Export Device to the United States But Perform No Other Operation on Device; Develop Specifications But Do Not Manufacture At This Facility; Manufacture Medical Device
Owner/operator: Stomatotech (#10046960)

Address: 4919 Boul St Charles, Pierrefonds Quebec, H9H 3E4, CA

Mandatory US Agent: Registrar corp

## Products

Total registered: 1
Top product codes: QRQ
Regulation §: 872.3980

Proprietary names: Crown Down Drilling Kit

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223010966817%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3010966817