Anax Dent G M B H

FDA Filings

This page includes the latest FDA filings for Anax Dent G M B H. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3007791519
FEI Number3007791519
NameTay Harvey
Owner & Operatoranax dent GmbH
Contact AddressOlgastrasse 120 A
Stuttgart DE-BW Baden-Wurttemberg 70180 DE
Official Correspondent
  • Andreas Kopietz
  • 049-711-6200920-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address406
Ardmore, OK 73401 US
Establishment TypeManufacture Medical Device

FDA Filings

Device
Company
DeviceDate
Tay Harvey [anax dent GmbH]
HansZahn2013-05-30
Tay Harvey [anax dent GmbH]
PMMA BLANKS2013-05-30
Tay Harvey [anax dent GmbH]
Visco III2013-05-30
Tay Harvey [anax dent GmbH]
anaxPINK2012-02-02
Tay Harvey [anax dent GmbH]
anaxGUM2012-02-02
Tay Harvey [anax dent GmbH]
anaxBLEND2012-02-02
Tay Harvey [anax dent GmbH]
Acryline2009-11-26
Tay Harvey [anax dent GmbH]
anaxGLAZE2009-02-20
Tay Harvey [anax dent GmbH]
New Outline2009-02-20

Similar & Related FDA Registered Companies

Related Finance Registrations
NCAGE CodeCL915ANAX DENT GMBH
CAGE CodeCL915ANAX DENT GMBH
U.S. Import Records [external site]
Import IDShipmentCargo DescriptionQuantity
2020080150150Stadersand,Federal Republic of Germany -> Houston, TexasSILICONE PUTTY HS CODE 39100000 AMS HBL DFW202393 SCAC SSLL3 PKG
2018031936371Bremerhaven,Federal Republic of Germany -> New York/Newark Area, Newark, New JerseySILICONE IN PRIMARY FORMHSCODE 39100000196 DRM
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.