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FDA 510(k) Applications for Medical Device Product Code "NTK"
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| FDA 510(k) Number | Applicant | Device Name | Decision Date |
| K062961 | ADDENT, INC. | MICROLUX TRANSILLUMINATOR | 02/08/2007 |
| K240573 | Align Technology Ltd. | iTero LuminaÖ Pro | 08/16/2024 |
| K193659 | Align Technology, Inc. | iTero Element 5D | 03/20/2020 |
| K213482 | D4D Technologies, LLC | TIA Tip, Cariosity, Transillumination Accessory Tip | 04/29/2022 |
| K172007 | Duerr Dental AG | CamX Triton HD Proxi Head | 11/22/2017 |
| K043068 | ELECTRO-OPTICAL SCIENCES, INC. | DIFOTI USB 2.0 SYSTEM | 12/29/2004 |
| K182712 | Kaltenbach & Voigt GmbH | DEXIS CariVu 3-in-1 by KaVo | 11/23/2019 |
| K123402 | KALTENBACH & VOIGT GMBH | DIAGNOCAM | 09/24/2013 |
| K060080 | KAVO DENTAL CORPORATION | DIAGNODENT 2190 WITH PERIODONTAL PROBE | 02/08/2006 |
| K071429 | KERR CORPORATION | TI2200 TRANSILLUMINATION CABLE | 09/10/2007 |