Cleared Traditional

Enhanced Handheld Pain Relief Laser Instrument (GD-P-E)

K241057 · Wuhan Guangdun Technology Co.,Ltd.. · Physical Medicine

Jan 2025

Decision

281d

Days

Class 2

Risk

About This 510(k) Submission

K241057 is an FDA 510(k) clearance for the Enhanced Handheld Pain Relief Laser Instrument (GD-P-E), a Powered Light Based Laser Non-thermal Instrument With Non-heating Effect For Adjunctive Use In Pain Therapy (Class II — Special Controls, product code NHN), submitted by Wuhan Guangdun Technology Co.,Ltd.. (Wuhan, CN). The FDA issued a Cleared decision on January 24, 2025, 281 days after receiving the submission on April 18, 2024. This device falls under the Physical Medicine review panel. Regulated under 21 CFR 890.5500.

Submission Details

510(k) Number	K241057 FDA.gov
FDA Decision	Cleared SESE
Date Received	April 18, 2024
Decision Date	January 24, 2025
Days to Decision	281 days
Submission Type	Traditional
Review Panel	Physical Medicine (PM)
Summary	Summary PDF

Device Classification

Product Code	NHN — Powered Light Based Laser Non-thermal Instrument With Non-heating Effect For Adjunctive Use In Pain Therapy
Device Class	Class II — Special Controls
CFR Regulation	21 CFR 890.5500
Definition	A Laser (light Amplification By Stimulated Emission Of Radiation) Based Device Having Coherence, Collimated And Typically Monochromatic Radiation. This Device Emits Energy In The Infrared Or Other Wavelengths, Provides Non-heating And Non-thermal Effect, And Is Indicated For Adjunctive Use In Pain Therapy Or Related Indication. It Does Not Provide Therapeutic Topical Heating. The Classification Regulation For Infrared Lamps Describes A Device That Emits Energy In The Infrared Wavelength To Provide Topical Heating And That Is Not Limited To Adjunctive Use.