Ambroise

FDA Filings

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

FDA Registration(s)
Registration Number3003883662
FEI Number3003883662
NameAMBROISE
Owner & OperatorAMBROISE
Contact AddressTwekkeler Es 24 --
ENSCHEDE NL-NOTA NL7547 SM NL
Official Correspondent
  • N.G.A. VAN - LEERDAM
  • 31-53-4302836-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressTwekkeler Es 24
ENSCHEDE Overijssel, NL7547 SM NL
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
AMBROISE
Wilmer Stretching Orthosis1997-08-21
AMBROISE
Wilmer Elbow Orthosis1997-08-21
AMBROISE
Wilmer Carrying Orthosis1997-08-21
AMBROISE
WSO1997-08-21
AMBROISE
WEO1997-08-21
AMBROISE
WCO1997-08-21
AMBROISE
Ambroise Dynamic Wrist Orthosis1997-08-21
AMBROISE
Ambroise Arm Orthosis1997-08-21
AMBROISE
ADPO1997-08-21
AMBROISE
UTX1997-08-21
AMBROISE
Radix1997-08-21
AMBROISE
Genux1997-08-21
AMBROISE
Dynko1997-08-21

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