Medical Diode Laser Systems (BERYLAS-12N); Medical Diode Laser Systems (BERYLAS-15N); Medical Diode Laser Systems (HARLAS-45JN); Medical Diode Laser Systems (HARLAS-46JN)

FDA 510(k) K252063 · Wuhan Dimed Laser Technology Co., Ltd.

Substantially Equivalent

510(k) numberK252063

Submission

Device name
Medical Diode Laser Systems (BERYLAS-12N); Medical Diode Laser Systems (BERYLAS-15N); Medical Diode Laser Systems (HARLAS-45JN); Medical Diode Laser Systems (HARLAS-46JN)
Applicant
Wuhan Dimed Laser Technology Co., Ltd.
Wuhan, CN
Received
July 1, 2025
Decision date
September 25, 2025
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
GEX – Powered Laser Surgical Instrument
Device class
Class II (moderate risk)
Regulation
21 CFR 878.4810
Specialty
General, Plastic Surgery

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…

Other 510(k)s with product code GEX

510(k)DeviceApplicantDecision
K262426Medical Diode Laser (S1Pro+, S1Pro K15, S1Pro N6, S1Pro N75)GEX · Traditional Wuhan Pioon Technology Co., Ltd.09/10/2026SE
K261562Diode Laser Therapy SystemGEX · Traditional Sanhe LEFIS Electronics Co., Ltd.09/10/2026SE
K2615891927nm Thulium Laser System (PZ-DJG85-01, PZ-DJG85-02)GEX · Traditional Zhengzhou PZ Laser Slim Technology Co., Ltd.09/02/2026SE
K262269CO2 Laser System (MBT- CO2 Laser)GEX · Traditional Beijing Mega Beauty Technology Co., Ltd.09/01/2026SE
K2618211565nm Laser Therapy Device (PZ-JG86-01,PZ-JG86-02)GEX · Traditional Zhengzhou PZ Laser Slim Technology Co., Ltd.08/27/2026SE
K262070Diode Laser Therapy Systems (DL612A)GEX · Traditional Hebei Zollvan Medical Technology Co., Ltd.08/19/2026SE
K261964Echolaser X4GEX · Traditional Elesta S.P.A08/19/2026SE
K261841Q Switched Nd:YAG Laser machine (QLQW-01)GEX · Traditional Beijing Nubway S&T Co., Ltd.08/11/2026SE
K261221SOLTIVE™ Laser System (SOLTIVE™ Pro SuperPulsed Laser, SOLTIVE™ Premium SuperPulsed…GEX · Traditional Olympus Surgical Technologies America07/24/2026SE
K261738Medical Thulium Fiber Laser Systems (UroFiber 150Q)GEX · Traditional Rhein Laser Technologies Co., Ltd.07/21/2026SE

More from Rhein Laser Technologies Co., Ltd.

510(k)DeviceDecision
K211977Medical Diode Laser SystemsGEX · Traditional 10/26/2021SE

Questions and answers

When was Medical Diode Laser Systems (BERYLAS-12N); Medical Diode Laser Systems (BERYLAS-15N); Medical Diode Laser Systems (HARLAS-45JN); Medical Diode Laser Systems (HARLAS-46JN) cleared by the FDA?

Medical Diode Laser Systems (BERYLAS-12N); Medical Diode Laser Systems (BERYLAS-15N); Medical Diode Laser Systems (HARLAS-45JN); Medical Diode Laser Systems (HARLAS-46JN) (K252063) received a 510(k) decision of Substantially Equivalent on September 25, 2025, 86 days after the submission was received.

What is the product code of K252063?

The FDA product code is GEX – Powered Laser Surgical Instrument, a Class II (moderate risk) device regulated under 21 CFR 878.4810.