Karen Vanderbosch

FDA Filings

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

FDA Registration(s)
Registration Number3007334667
FEI Number3007334667
NameKAREN VANDERBOSCH
Owner & OperatorGLOBAL MANUFACTURING GROUP LIMITED
Contact AddressRM 1613, 16/F, TREND CENTRE 29 CHEUNG LEE STREET, CHAIWAN
HONG KONG HK-NA 852 HK
Official Correspondent
  • KIM - MAN-WAI PANG
  • 852-246-09016-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address1021 BANDANA BOULEVARD EAST, SUITE 220, SAINT PAUL
Saint Paul, MN 55108 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
KAREN VANDERBOSCH [GLOBAL MANUFACTURING GROUP LIMITED]
VULKAN2003-05-05
KAREN VANDERBOSCH [GLOBAL MANUFACTURING GROUP LIMITED]
ERGODYNE PROFLEX2003-05-05

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