Dentec, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
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Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K894930 | DENTEC 4000 | ETN | 1990-03-27 | View |
| 510(k) | K864376 | FIBERBOND | DYT | 1987-04-07 | View |
| 510(k) | K833429 | PERI MIRROR/SALIVA EJECTOR | EAX | 1983-12-22 | View |
No matching devices.
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