Christy Foreman

FDA Filings

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

FDA Registration(s)
Registration Number3014326253
FEI Number3014326253
NameChristy Foreman
Owner & OperatorReapplix
Contact AddressBlokken 45
Birker?d DK-85 Region Sjaelland 3460 DK
Official Correspondent
  • Niels Erik Holm
  • 45-26-221962-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address1555 King Street, Suite 300
Alexandria, VA 22314 US
Establishment TypeManufacture Medical Device

FDA Filings

Device
Company
DeviceDate
Christy Foreman [Reapplix]
3CP Counterbalance2018-03-01
Christy Foreman [Reapplix]
3CP Centrifuge2018-03-01
Christy Foreman [Reapplix]
3C Patch System2018-03-01
Christy Foreman [Reapplix]
3C Patch System2018-03-01
Christy Foreman [Reapplix]
3C Patch Needle Holder2018-03-01
Christy Foreman [Reapplix]
3C Patch Kit2018-03-01
Christy Foreman [Reapplix]
3C Patch Device2018-03-01

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