Ab Ardent
FDA 510(k) & PMA Approved Devices — 13 products
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Total Devices13
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K131753 | MERIDIAN | EBF | 2013-11-14 | View |
| 510(k) | K040465 | LATIT FLOW | EBF | 2004-07-20 | View |
| 510(k) | K022971 | MICROHYBRID 11 | EBF | 2002-11-25 | View |
| 510(k) | K022973 | ADHESIVE 14 | KLE | 2002-11-22 | View |
| 510(k) | K022972 | MICROFILL 13 | EBF | 2002-11-22 | View |
| 510(k) | K022975 | ETCHING 15 | EBF | 2002-11-22 | View |
| 510(k) | K022974 | MICROHYBRID 12 | EBF | 2002-11-22 | View |
| 510(k) | K020452 | HIGH SILVER CONVENTIONAL | EJJ | 2002-05-07 | View |
| 510(k) | K011801 | FUTURA TOPCAP NON GAMMA-2 | EJJ | 2001-08-16 | View |
| 510(k) | K991974 | FUTURA GLASS IONOMER SILVER REINFORCED | EMA | 1999-09-17 | View |
| 510(k) | K982460 | VIVACAP HR | EJJ | 1998-08-24 | View |
| 510(k) | K982458 | VIVALLOY HR | EJJ | 1998-08-24 | View |
| 510(k) | K982456 | AMALCAP PLUS | EJJ | 1998-08-24 | View |
No matching devices.
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