SOGA Lasers therapy system family of Aurora handpiece (Aurora-S); SOGA Lasers therapy system family of the Dental diode laser ( ILaser III Pro)

FDA 510(k) K253309 · Shenzhen Soga Technology Co., Ltd.

Substantially Equivalent

510(k) numberK253309

Submission

Device name
SOGA Lasers therapy system family of Aurora handpiece (Aurora-S); SOGA Lasers therapy system family of the Dental diode laser ( ILaser III Pro)
Applicant
Shenzhen Soga Technology Co., Ltd.
Shenzhen, CN
Received
September 29, 2025
Decision date
May 19, 2026
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
NVK – Laser, Dental, Soft Tissue
Device class
Class II (moderate risk)
Regulation
21 CFR 878.4810
Specialty
General, Plastic Surgery

Intended for the incision, excision, cutting, ablation, and vaporization of soft tissue in oral and maxillofacial surgery and dentistry.

Other 510(k)s with product code NVK

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K260765Gemini NOVA 810+980 Soft Tissue LaserNVK · Traditional Azena Medical, LLC03/10/2026SE
K250731MateLaser Medical Diode Laser Systems (ML-DLS-30)NVK · Traditional Matelaser, Inc.10/16/2025SE
K243764Medical Diode Laser (UTU3-F7B,UTU3-F7W,UTU3-G7B,UTU3-G7W,UTU-G20B,UTU-G20W)NVK · Traditional Wuhan Pioon Technology Co., Ltd.05/08/2025SE
K230047Medical Diode Laser SystemsNVK · Traditional Gigaalaser Company , Ltd.03/04/2024SE
K232885Dawn Diode Laser SystemNVK · Traditional Shanghai Wonderful Opto-Electrics Tech.Co.,Ltd02/28/2024SE
K232222Primo Dental Laser (Primo, Primo Komfort, Primo Lite, Primo Blue, and Primo Triplo)NVK · Traditional Medency S.R.L.11/27/2023SE
K221761SoleaNVK · Traditional Convergent Dental, Inc.09/14/2022SE
K211150Dental diode laser, SOGA Laser, ILaser IINVK · Abbreviated Shenzhen Soga Technology Co., Ltd.07/01/2022SE
K214008Dental diode laserNVK · Abbreviated Shenzhen Soga Technology Co., Ltd.05/10/2022SE
K213658Deka SmartperioNVK · Special El.En Electronic Engineering Spa03/11/2022SE

More from El.En Electronic Engineering Spa

510(k)DeviceDecision
K211150Dental diode laser, SOGA Laser, ILaser IINVK · Abbreviated 07/01/2022SE
K214008Dental diode laserNVK · Abbreviated 05/10/2022SE

Questions and answers

When was SOGA Lasers therapy system family of Aurora handpiece (Aurora-S); SOGA Lasers therapy system family of the Dental diode laser ( ILaser III Pro) cleared by the FDA?

SOGA Lasers therapy system family of Aurora handpiece (Aurora-S); SOGA Lasers therapy system family of the Dental diode laser ( ILaser III Pro) (K253309) received a 510(k) decision of Substantially Equivalent on May 19, 2026, 232 days after the submission was received.

What is the product code of K253309?

The FDA product code is NVK – Laser, Dental, Soft Tissue, a Class II (moderate risk) device regulated under 21 CFR 878.4810.