TüVRheinland
Verificación in situ por líder Mundial de Empresa TUV Group
ISO 13485:2016,US FDA, Medical CE, MDSAP Certified
Safety and quality are non-negotiable in beauty machine industry .
Weifang KM is ISO 13485:2016, US FDA, Medical CE, MDSAP certified. It means that our factoryis involved in the design, production, installation and after service for the diode laser machines.
As an ISO 13485:2016, US FDA, Medical CE, MDSAP certified manufacturer, our state of the art facility must be able to demonstrate our quality management processes and ensure best practice in everything we do, in order to meet this highly regulated standard. Quality and safety always our target!
Our Innovation
Machine quality is defined by hardware and software, working harmoniously together to offer superior treatment results and we continue to refine this experience to offer an intuitive user interface that simplifies the operation for the technician.
Innovative technology, branded parts, such as Italy water pump, USA Coherent laser bars etc, beautiful design and quality build- This has dramatically pushed the boundaries for our machines, leading Weifang KM Laser into a new era of Laser precision.
Company history
Company history
2009
06-08
Established a factory to produce cavitation RF, IPL/Elight, Nd yag laser, lipo laser machine.
2013
03-06
A new office block was built, and create R&D department, program department. At the same time, we got ITC Medical CE,and ISO13485
2015
06-09
Bring 808nm diode laser machine, fractional Co2 laser machine, Velashape machine to the market.
2018
08
Finally got Germany TUV issued Medical CE, ISO13485 and ISO9001
2019
07
We got US FDA and Australia TGA approval for diode laser hair removal machine
2020
12
We won the national high-tech enterprise certification
2021
01
We got the Canada MDSAP approval, and more than 100 distributors from all over the world
Get a incomparable result with Weifang KM FDA, Medical CE approved diode laser machine
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