Medshift

FDA Filings

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

FDA Registration(s)
Registration Number3013462594
FEI Number3013462594
NameMedShift
Owner & OperatorMedShift
Contact Address525 N Tryon St Suite 1600
Charlotte NC 28202 US
Official Correspondent
  • Brian Phillips
  • 1-800-9800522-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address851 Blairhill Road
Charlotte, NC 28217 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
MedShift
MedShift IoT - Connected Device2019-11-12

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