Somnomed, Inc.
FDA 510(k) & PMA Approved Devices — 9 products
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Total Devices9
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K261366 | Virtus | LRK | 2026-06-12 | View |
| 510(k) | K233497 | Rest Assure System | PLC | 2024-10-03 | View |
| 510(k) | K183443 | SomnoDent Avant | LRK | 2019-05-08 | View |
| 510(k) | K162306 | SomnoDent ALPHA | LRK | 2016-09-20 | View |
| 510(k) | K130558 | SOMNODENT HERBST; CLASSIC, FLEX | LRK | 2013-05-17 | View |
| 510(k) | K121340 | SOMNODENT G2 | LRK | 2012-05-30 | View |
| 510(k) | K102909 | SOMNOBRUX SPLINTS | MQC | 2011-12-13 | View |
| 510(k) | K102521 | PANTINO PRO POSITINER | LRK | 2011-03-28 | View |
| 510(k) | K073004 | SOMNOMED BFLEX | LRK | 2008-01-30 | View |
No matching devices.
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