Criterion Tool Die Inc

FDA Filings

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

FDA Registration(s)
Registration Number1528668
FEI Number1000136409
NameCRITERION TOOL & DIE INC
Owner & OperatorCRITERION TOOL & DIE INC
Contact Address5349 WEST 161ST ST. --
Brook Park OH 44142 US
Official Correspondent
  • TANYA - DISALVO
  • x-216-2671733-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address5349 W 161st St
BROOK PARK, OH 44142 US
Establishment TypeManufacture Medical Device for Another Party (Contract Manufacturer)



FDA Filings

Device
Company
DeviceDate
CRITERION TOOL & DIE INC
Orthodepic Manual Surgical Instrument2017-05-15
CRITERION TOOL & DIE INC
Guide, surgical, instrument2017-05-15
CRITERION TOOL & DIE INC
ATS cylindrical cuff,single prort/dual bladder2013-01-23

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