Ultrasonic Scaler (WD-JY-B002,WD-JY-W001,WD-JY-R003,WD-JY-G004,WD-JY-B003,WD-JY-C006,WD-JY-M0014, WD-JY-N0015,WD-JY-N0016,WD-JY-N0017,WD-JY-E007, WD-JY-F008,WD-JY-A005,WD-JY-H009,WD-JY-I0011, WD-JY-K0012,WD-JY-K0013,WD-JY-K0014, WD-JY-L0013,WD-JY-L0014,WD-JY-L0015, WD-JY-L0016,WD-JY-L0017)
K240707 is the FDA 510(k) clearance record for Ultrasonic Scaler (WD-JY-B002,WD-JY-W001,WD-JY-R003,WD-JY-G004,WD-JY-B003,WD-JY-C006,WD-JY-M0014, WD-JY-N0015,WD-JY-N0016,WD-JY-N0017,WD-JY-E007, WD-JY-F008,WD-JY-A005,WD-JY-H009,WD-JY-I0011, WD-JY-K0012,WD-JY-K0013,WD-JY-K0014, WD-JY-L0013,WD-JY-L0014,WD-JY-L0015, WD-JY-L0016,WD-JY-L0017), a class II device, cleared for Shenzhen Micro Electric Intelligence Co., Ltd. on under FDA product code ELC (Scaler, Ultrasonic). FDA records list one 510(k) clearance for Shenzhen Micro Electric Intelligence Co., Ltd. As of , FDA records show no recalls naming K240707.
Clearance record
- Decision date
- Received
- (109 days to decision)
- Product code
- ELC Scaler, Ultrasonic
- Regulation
- 21 CFR 872.4850
- Device class
- Class II
- Review panel
- Dental
- Applicant
- Shenzhen Micro Electric Intelligence Co., Ltd. 301, Bldg. A5, # 13 Baonan Rd., Longgang Community, Shenzhen, CN
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code ELC
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 0 |
| January 2026 | 1 |
| February 2026 | 0 |
| March 2026 | 1 |
| April 2026 | 0 |
| May 2026 | 0 |
| June 2026 | 0 |
| July 2026 | 0 |
| August 2026 | 0 |
| September 2026 | 0 |
| October 2026 | 0 |
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