Handi Craft Co Saint Louis

FDA Filings

This page includes the latest FDA filings for Handi Craft Co Saint Louis. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3008138005
FEI Number3008138005
NameHandi-Craft Co -Saint Louis
Owner & OperatorHandi-Craft Co
Contact Address4433 Fyler Ave.
Saint Louis MO 63116 US
Official Correspondent
  • Kelly Kane
  • x-314-4453381-x
Registration Status1
Initial ImporterY
Registration Expiration2020-04-25
Registration Address4433 Fyler Ave.
Saint Louis, MO 63116 US
Establishment Type
  • Develop Specifications But Do Not Manufacture At This Facility
  • Repack or Relabel Medical Device

FDA Filings

Device
Company
DeviceDate
Handi-Craft Co -Saint Louis [Handi-Craft Co]
Dr. Brown's2016-06-22
Handi-Craft Co -Saint Louis [Handi-Craft Co]
Dr. Browns2014-12-22
Handi-Craft Co -Saint Louis [Handi-Craft Co]
Dr. Browns2014-12-22

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