Levo Ag

FDA Filings

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

FDA Registration(s)
Registration Number9681680
FEI Number1000268398
NameLEVO AG
Owner & OperatorDANE TECHNOLOGIES
Contact Address10400 Fountains Drive --
Maple Grove MN 55369 US
Official Correspondent
  • Amy L Jorgensen
  • x-763-7461153-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressANGLIKERSTRASSE 20
WOHLEN Aargau, CH-5610 CH
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
LEVO AG [DANE TECHNOLOGIES]
LEVO MAX 3002015-03-20
LEVO AG [DANE TECHNOLOGIES]
LEVO MAX 2002015-03-20
LEVO AG [DANE TECHNOLOGIES]
LEVO MAX 1002015-03-20
LEVO AG
LEVO MAX2015-01-21
LEVO AG [DANE TECHNOLOGIES]
C32011-03-16
LEVO AG
LEVO C32008-10-24
LEVO AG [DANE TECHNOLOGIES]
LCE/LCEV/KID/JR2007-11-01
LEVO AG [DANE TECHNOLOGIES]
LAE2007-11-01
LEVO AG [DANE TECHNOLOGIES]
LCM2007-11-01
LEVO AG [DANE TECHNOLOGIES]
LC2007-11-01
LEVO AG [DANE TECHNOLOGIES]
Comfort II2007-11-01
LEVO AG [DANE TECHNOLOGIES]
Combi/Combi JR2007-11-01
LEVO AG
LEVO COMFORT II2005-06-10
LEVO AG
LEVO COMBI2003-04-02

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