Ivylaser (Beijing) Technology Co., Ltd.

Registered establishment in Beijing, China. 2 device types, 3 clearances.

Registry build 21.09.26

Ivylaser (Beijing) Technology Co., Ltd. is a manufacturer holding a current FDA establishment registration. The registration covers Powered Laser Surgical Instrument, Light Based Over-The-Counter Hair Removal. Its earliest product listing with the FDA dates from 2023.

2device types registered with the FDA
3510(k) clearances

Registration

FDA registration record for Ivylaser (Beijing) Technology Co., Ltd.
Registered name IVYLASER (BEIJING) TECHNOLOGY CO., LTD.
Status Registered
Registration expires 2026
Registration number 3013446079
FEI number 3013446079
Establishment type Manufacturer

Chinese Registration

Chinese company register details for Ivylaser (Beijing) Technology Co., Ltd.
Chinese legal name 北京强光爱维科技有限公司
Source customs registration record

Location

Address of Ivylaser (Beijing) Technology Co., Ltd.
City Beijing
Province Beijing
Address Room 411, Building 3, No. 2 Shengfang Road, Daxing District, Beijing
Postal code 102600
Country China

What It Makes

Device types Ivylaser (Beijing) Technology Co., Ltd. is registered to make
Device type Class Listed under the names Listed since Chinese makers
Light Based Over-The-Counter Hair Removal Class 2 IVYLASER Handhold Hair Removal Machine 2023 69
Powered Laser Surgical Instrument Class 2 Diode laser system(Predator), Diode laser system(Night Universe), IVYLASER Diode laser hair removal system(IVY-HR-Alloy) 2024 92

Clearances

510(k) clearances naming Ivylaser (Beijing) Technology Co., Ltd. or its listings
Clearance Decision date Product code Route Held by
K250206 2025-04-24 GEX Traditional This company
K240611 2024-06-20 GEX Traditional This company
K230025 2023-07-03 OHT Traditional This company

From the Company

Published by the company on its own website, not by the FDA.

Information published by Ivylaser (Beijing) Technology Co., Ltd.
Founded 2008
Main products Laser hair removal systems, Body contouring units, Laser aesthetics machines
Certifications CE, FDA K250206, ISO 13485, High-Tech Enterprise

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Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

The manufacturer named here can complete this record.

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