510(k) K240482

Device
Intense Pulsed Light System (ST-690)
Applicant
Smedtrum Medical Technology Co., Ltd.
510(k) number
K240482
Product code
ONF
Decision
Substantially Equivalent (SESE)
Decision date
2024-05-17
Date received
2024-02-20
Regulation
878.4810
Classification name
Powered Light Based Non-Laser Surgical Instrument With Thermal Effect
Medical specialty
General, Plastic Surgery
Review panel
General, Plastic Surgery
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Crimson Wu
Address
1f., # 8, Ln. 97, Wugong Rd., Xinzhuang Dist. New Taipei City TW 248016 248016

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

Other 510(k) Records For Product Code ONF

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K251545Intense Pulsed Light Therapy Device (MMABM-1)Micowey Medical Equipment (Guangxi) Co., Ltd.2025-09-04
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K233473DEKA LOTUSEl.En S.P.A.2024-05-16
K233307Intensity Pulsed Light Therapy SystemBeijing Adss Development Co., Ltd.2024-03-15
K232708Intense pulsed light therapy deviceHebei Zhemai Technology Co., Ltd.2023-12-01
K232192Venus Versa PRO SystemVenus Concept, Inc.2023-09-11
K231394Intense Pulsed Light SystemSmedtrum Medical Technology Co., Ltd.2023-08-09
K230816Intense Pulsed Light Treatment SystemShangdong Huamei Technology Co., Ltd.2023-04-21
K220214Painless IPL System - KDT750Shanghai Omni Laser Skinology Co., Ltd.2023-02-18
K22079410PLTentech Co. , Ltd.2022-11-10
K221214Hand-held IPL device (IPL Home Use Hair Removal Device) Model:FZ-608, FZ-608G, FZ-100, FZ-200Shenzhen Ionka Medical Technology Co., Ltd.2022-09-21