Hospitec Usa

FDA Filings

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

FDA Registration(s)
Registration Number3008009298
FEI Number3008009298
NameHospitec USA
Owner & OperatorHospitec USA
Contact Address3730 Wheeler Ave
Fort Smith AR 72901 US
Official Correspondent
  • Ryan Embree
  • x-469-6676406-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address3730 Wheeler Ave
Fort Smith, AR 72901 US
Establishment TypeDevelop Specifications But Do Not Manufacture At This Facility



FDA Filings

Device
Company
DeviceDate
Hospitec USA
Medi Bulter2009-10-05

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