Dio Department Dsi, Inc.
FDA 510(k) & PMA Approved Devices — 8 products
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Total Devices8
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K080129 | SECURE IMPLANT SYSTEM (2.5/3.0MM) | DZE | 2008-05-30 | View |
| 510(k) | K073070 | DIO BIOTITE-H IMPLANT SYSTEM | DZE | 2008-05-16 | View |
| 510(k) | K080128 | SM-EXTRA WIDE (RBM) IMPLANT SYSTEM | DZE | 2008-05-14 | View |
| 510(k) | K070570 | DIO IMPLANT SYSTEM | DZE | 2008-04-15 | View |
| 510(k) | K080126 | DIO PROTEM IMPLANT SYSTEM | DZE | 2008-04-11 | View |
| 510(k) | K070569 | SM INTERNAL./EXTERNAL IMPLANT SYSTEM | DZE | 2007-11-08 | View |
| 510(k) | K070568 | DIO PROTEM IMPLANT SYSTEM | DZE | 2007-05-25 | View |
| 510(k) | K061797 | SM IMPLANT SYSTEMS | DZE | 2006-09-01 | View |
No matching devices.
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