Dentatus USA , Ltd.
FDA 510(k) & PMA Approved Devices — 4 products
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Total Devices4
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K042931 | TUF LINK SILICONE RELINER | EBI | 2004-12-08 | View |
| 510(k) | K031793 | DENTATUS OSCIOMAT | DZH | 2003-11-13 | View |
| 510(k) | K980620 | DENTATUS MTI MODULAR TRANSITIONAL IMPLANTS AND PROSTHETIC SYSTEM | DZE | 1998-05-15 | View |
| 510(k) | K961704 | MTI-MP TRANSITIONAL IMPLANTS AND MODULAR PROSTHETIC SYSTEM | ELS | 1996-07-26 | View |
No matching devices.
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