Phillibert

FDA Filings

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

FDA Registration(s)
Registration Number3006356395
FEI Number3006356395
NamePHILLIBERT
Owner & OperatorINDORO FRANCE
Contact Address250 Rue des Freres Lumiere 39000 Lons le Saunier
France FR-NOTA 393000 FR
Official Correspondent
  • TANG WAN - CHING
  • 33-384-2563-63
US Agent
Importing Logistics Registration
ImporterZHANGMUTAU LOGIEN OPTICAL FACTORY
AddressZHANGMUTOU ZHEN, ZHANG LUO, GUAN LI QU DONGGUAN, GUANGDONG.
CHINA, 86 CHINA
Importer TypeEnd User
SubdivisionCN-44
Importing Logistics Registration
ImporterZHANGMUTAU LONGIEN OPTICAL FACTORY
AddressZHANGMUTOU ZHEN LUO, GUAN LI QU DONGGUAN, GUANGDONG
CHINA, 86 CHINA
Importer TypeEnd User
SubdivisionCN-44
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address215 WESTLAND CIR. WOODWAY,
Waco, TX 76712 US
Establishment TypeManufacture Medical Device

FDA Filings

Device
Company
DeviceDate
PHILLIBERT [INDORO FRANCE]
SUNGLASSES (NON-PRESCRIPTION)2007-06-15

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