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.
Registration Number | 3006356395 | ||||||||
FEI Number | 3006356395 | ||||||||
Name | PHILLIBERT | ||||||||
Owner & Operator | INDORO FRANCE | ||||||||
Contact Address | 250 Rue des Freres Lumiere 39000 Lons le Saunier France FR-NOTA 393000 FR | ||||||||
Official Correspondent |
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US Agent |
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Importing Logistics Registration |
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Importing Logistics Registration |
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Registration Status | 1 | ||||||||
Initial Importer | N | ||||||||
Registration Expiration | 2020-04-25 | ||||||||
Registration Address | 215 WESTLAND CIR. WOODWAY, Waco, TX 76712 US | ||||||||
Establishment Type | Manufacture Medical Device |
Device Company | Device | Date |
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PHILLIBERT [INDORO FRANCE] | SUNGLASSES (NON-PRESCRIPTION) | 2007-06-15 |