K242892 is an FDA 510(k) clearance for the Cristaline Aligners Z FLX. This device is classified as a Aligner, Sequential (Class II - Special Controls, product code NXC).
Submitted by Cristaline Aligners GmbH (Pforzheim, DE). The FDA issued a Cleared decision on December 19, 2024, 87 days after receiving the submission on September 23, 2024.
This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.5470. The Device Moves The Teeth By Continuous Gentle Force For Treatment Of Minor Tooth Malocclusion..
| 510(k) Number | K242892 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | September 23, 2024 |
| Decision Date | December 19, 2024 |
| Days to Decision | 87 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | Summary PDF |
| Product Code | NXC - Aligner, Sequential |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 872.5470 |
| Definition | The Device Moves The Teeth By Continuous Gentle Force For Treatment Of Minor Tooth Malocclusion. |