Medart A S

FDA Filings

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

FDA Registration(s)
Registration Number8021543
FEI Number3005616124
NameMEDART A/S
Owner & OperatorMEDART A/S
Contact AddressIndustriholmen 15A --
HVIDOVRE DK-84 Region Hovedstaden DK-2650 DK
Official Correspondent
  • OLAV - BALLE-PETERSEN
  • 45-363-42300-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressINDUSTRIHOLMEN 15A
HVIDOVRE Region Hovedstaden, DK-2650 DK
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
Medart A/S
MedArt Intenz 620.0002019-02-07
MEDART A/S
MedArt 4592013-02-15
MEDART A/S
MedArt 4582013-02-15
MEDART A/S
MedArt 4132013-02-15
MEDART A/S
MedArt Intenz2013-02-15
MEDART A/S
MedArt 6202013-02-15
MEDART A/S
MedArt FRx2013-02-15
MEDART A/S
MedArt 6102013-02-15
MEDART A/S
MedArt 5252013-02-15
MEDART A/S
MEDART 6202012-06-13
MEDART A/S
MedArt 7202011-07-08
MEDART A/S
MedArt 9542011-07-08
MEDART A/S
Ellipse Juvia2011-07-08
MEDART A/S
MEDART DIODE LASER SYSTEM & ACCESSORIES2011-06-28
MEDART A/S
MEDART MODEL 610 CO2 LASER SYSTEM & ACCESSORIES2009-11-24
MEDART A/S
MedArt430 MedArt4352007-12-19
MEDART A/S
MedArt VariMed2007-12-19
MEDART A/S
MedArt 9352007-12-19
MEDART A/S
MedArt450 MedArt6102007-12-19
MEDART A/S
MedArt FRx2007-12-19

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