Clearance Summary
Medical Diode Laser (S1Pro+, S1Pro K15, S1Pro N6, S1Pro N75) received FDA 510(k) clearance under submission number K262426, sponsored by Wuhan Pioon Technology Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2026-09-10.
- Submission: K262426
- Applicant / Sponsor: Wuhan Pioon Technology Co., Ltd.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4810
- Decision date: 2026-09-10
Classification & Regulation
This clearance is catalogued under FDA product code GEX and 21 CFR 878.4810, within the General, Plastic Surgery review panel as a Class II device.