510(k) K242637
K242637 is an FDA 510(k) premarket notification submitted by Mem Dental Technology Co., Ltd. for the device "MEM Clear Aligner System". The FDA issued a decision of Substantially Equivalent on May 21, 2025. The device falls under product code NXC (Aligner, Sequential), a Class II device regulated under 21 CFR 872.5470. Mem Dental Technology Co., Ltd. has at least 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 21, 2025
- Date Received
- September 3, 2024
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Aligner, Sequential
- Device Class
- Class II
- Regulation Number
- 872.5470
- Review Panel
- DE
- Submission Type
The device moves the teeth by continuous gentle force for treatment of minor tooth malocclusion.