510(k) K260179
K260179 is an FDA 510(k) premarket notification submitted by Touchbeauty Beauty & Health (Shenzhen) Co., Ltd. for the device "VITA Multi-Function Head Brush (TB-2343F, TB-2442F)". The FDA issued a decision of Substantially Equivalent on June 3, 2026. The device falls under product code NFO (Stimulator, Transcutaneous Electrical, Aesthetic Purposes), a Class II device regulated under 21 CFR 882.5890. Touchbeauty Beauty & Health (Shenzhen) Co., Ltd. has at least 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 3, 2026
- Date Received
- January 21, 2026
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Stimulator, Transcutaneous Electrical, Aesthetic Purposes
- Device Class
- Class II
- Regulation Number
- 882.5890
- Review Panel
- NE
- Submission Type