Align Technology , Ltd.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories1
Latest FDA decision2026-07-02
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K261847 | iTero Lumina™ Pro | NTK | 2026-07-02 | View |
| 510(k) | K240573 | iTero Lumina™ Pro | NTK | 2024-08-16 | View |
No matching devices.