Fussen Technology Co., Ltd.
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K263033 | Dental Computed Tomography X-ray System (Rubik XSmart, Rubik X1, Rubik X3) (Matrix 7000, Matrix 7800) | OAS | 2026-09-30 | View |
| 510(k) | K251842 | Dental Computed Tomography X-ray System | OAS | 2025-11-13 | View |
No matching devices.
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