Tritone Inc

FDA Filings

This page includes the latest FDA filings for Tritone Inc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

Tritone Inc holds import registrations or U.S. agent authorizations in conjunction with the following organizations:

FDA Registration(s)
Registration Number3012256357
FEI Number3012256357
NameTRITONE INC
Owner & OperatorTRITONE INC
Contact Address222 Merchandise Mart Plaza Suite 1225
Chicago IL 60654 US
Official Correspondent
  • Nabeel Athar
  • 1-773-9973421-x
Registration Status1
Initial ImporterY
Registration Expiration2020-04-25
Registration Address222 Merchandise Mart Plaza Suite 1225
Chicago, IL 60654 US
Establishment Type
  • Manufacture Medical Device for Another Party (Contract Manufacturer)
  • Develop Specifications But Do Not Manufacture At This Facility



FDA Filings

Device
Company
DeviceDate
TRITONE INC
TRITONE INC2020-04-08
TRITONE INC
Tischler Forcep2020-03-17
TRITONE INC
Scissors2016-02-22

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