Diode Laser System (5 models)— 510(k) K243141

Name: FDA 510(k) clearance K243141
Creator: U.S. Food and Drug Administration
Published: 2024-12-26

Substantially Equivalent

Jiangxi Medex Technology Co., Ltd.

FDA 510(k) clearance K243141 for Diode Laser System (5 models), Substantially Equivalent on 2024-12-26. Applicant: Jiangxi Medex Technology Co., Ltd.. Device class: 2.

Clearance details

Device name as filed: Diode Laser System (LaserPro D 980); Diode Laser System (LaserPro D 810); Diode Laser System (Aurolance 980); Diode Laser System (Aurolance 810); Diode Laser System (Aurolance AM)
Applicant: Jiangxi Medex Technology Co., Ltd.
Product code: Code GEX
Device class: Class 2
Regulation: 21 CFR 878.4810
Advisory panel: General, Plastic Surgery
Date received: 2024-09-30
Decision date: 2024-12-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Jiangxi, CN

Download summary PDF View on FDA.gov ↗

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Adverse events under product code GEX

product code GEX

Death: 33
Injury: 3,045
Malfunction: 12,903
Other: 25
Total: 16,006

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.