Cleared Traditional

Medical Diode Laser (S1Pro)

K240644 · Wuhan Pioon Technology Co., Ltd. · General & Plastic Surgery

Jun 2024

Decision

95d

Days

Class 2

Risk

About This 510(k) Submission

K240644 is an FDA 510(k) clearance for the Medical Diode Laser (S1Pro), a Powered Laser Surgical Instrument (Class II — Special Controls, product code GEX), submitted by Wuhan Pioon Technology Co., Ltd. (Wuhan, CN). The FDA issued a Cleared decision on June 10, 2024, 95 days after receiving the submission on March 7, 2024. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.4810.

Submission Details

510(k) Number	K240644 FDA.gov
FDA Decision	Cleared SESE
Date Received	March 07, 2024
Decision Date	June 10, 2024
Days to Decision	95 days
Submission Type	Traditional
Review Panel	General & Plastic Surgery (SU)
Summary	Summary PDF

Device Classification

Product Code	GEX — Powered Laser Surgical Instrument
Device Class	Class II — Special Controls
CFR Regulation	21 CFR 878.4810
Definition	A Laser (light Amplification By Stimulated Emission Of Radiation) Based Device Having Coherence, Collimated And Typically Monochromatic Radiation. Typically Indicated To To Cut, Destroy, Remove Or Coagulate Tissue, Generally Soft Tissue, For General Surgical Purpose In Medical Specialties Of General And Plastic Surgery, Dermatology/aesthetic, Podiatry, Otolaryngology (ent), Gynecology, Neurosurgery, Orthopedics (soft Tissue), Dental And Oral Surgery, And Dentistry. The Classification Regulation 21 Cfr 878.4810 Describes A Device That Is Carbon Dioxide Or Argon Laser Intended To Cut, Destroy, Remove Or Coagulate Tissue By The Light.