Medicraft Inc Creighton

FDA Filings

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

FDA Registration(s)
Registration Number3009538923
FEI Number3009538923
NameMedicraft Inc
Owner & OperatorMedicraft Inc/Creighton
Contact Address50 Bushes Lane
Elmwood Park NJ 07407 US
Official Correspondent
  • Shalyn Creighton
  • 1-201-7978820-101
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address50 Bushes Ln
Elmwood Park, NJ 07407 US
Establishment TypeManufacture Medical Device for Another Party (Contract Manufacturer)



FDA Filings

Device
Company
DeviceDate
Medicraft Inc [Medicraft Inc/Creighton]
Tray, Surgical, Instrument2020-04-08

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