Danielwei

FDA Filings

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

FDA Registration(s)
Registration Number3005202231
FEI Number3005202231
NameDANIELWEI
Owner & OperatorALLIED GROUP DEVELOPMENT LIMITED
Contact Address22A MING WAH IND. BLDG. 17-33 WANG LUNG STREET
TSUEN WAN, N.T. HK-NA -- HK
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address2920 PACIFIC DR
NORCROSS, GA 30071 US
Establishment Type
  • Manufacture Medical Device
  • Export Device to the United States But Perform No Other Operation on Device



FDA Filings

Device
Company
DeviceDate
DANIELWEI [ALLIED GROUP DEVELOPMENT LIMITED]
BestScale2019-12-03
DANIELWEI [ALLIED GROUP DEVELOPMENT LIMITED]
Transfer Sheet2006-05-11
DANIELWEI [ALLIED GROUP DEVELOPMENT LIMITED]
Sling2005-06-10
DANIELWEI [ALLIED GROUP DEVELOPMENT LIMITED]
Patient Lift2005-06-10

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