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 |
| ||||||||
| US Agent |
| ||||||||
| Importing Logistics Registration |
| ||||||||
| Importing Logistics Registration |
| ||||||||
| 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 |
|---|---|---|
PHILLIBERT [INDORO FRANCE] | SUNGLASSES (NON-PRESCRIPTION) | 2007-06-15 |