This page includes the latest FDA filings for Ab Ardent. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 9681880 |
| FEI Number | 3002512705 |
| Name | AB ARDENT |
| Owner & Operator | IVOCLAR VIVADENT AG |
| Contact Address | 175 Pineview Dr. Amherst NY 14228 US |
| Official Correspondent |
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| US Agent |
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| Registration Status | 1 |
| Initial Importer | N |
| Registration Expiration | 2020-04-25 |
| Registration Address | 8 GENERATORGATAN ARLANDASTAD Stockholms lan [SE-01], SE-195 60 SE |
| Establishment Type | Repack or Relabel Medical Device |
Device Company | Device | Date |
|---|---|---|
| AB Ardent | OPC 3G 629246 | 2018-07-24 |
AB ARDENT [IVOCLAR VIVADENT AG] | Illusion | 2013-11-21 |
AB ARDENT | MERIDIAN | 2013-11-14 |
AB ARDENT | LATIT FLOW | 2004-07-20 |
AB ARDENT | MICROHYBRID 12 | 2002-11-22 |
AB ARDENT | FUTURA GLASS IONOMER SILVER REINFORCED | 1999-09-17 |
AB ARDENT | VIVACAP HR | 1998-08-24 |
AB ARDENT | VIVALLOY HR | 1998-08-24 |
AB ARDENT | AMALCAP PLUS | 1998-08-24 |