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Shenzhen Leaflife Technology Co., Ltd., established in 2017 year, is located in Shenzhen city as the innovation capital of China. It is a high-tech company integrating R & D, manufacturing and marketing of professional medical, beauty and home use beauty equipment, technologies and services. 

The products are divided into medical laser equipment, beauty equipment, home use beauty equipment, and core components such as laser generator, chips. The products are sold to more than 80 countries around the world, with annual sales of more than RMB 80 million. The customers group contains powerful distributors in more countries, well-known hospitals and doctors, chain brand stores, including most competitive and advanced core components for brand equipment suppliers in china and abroad.

As a new high-tech company oriented by innovation, Leaflife has powerful R & D strength in the field. Lealife has pioneered fiber coupled diode laser and international patented LED hair removal technology, which lead new technological innovations and market upgrades worldwide. 

Latest cold and fractional Plasma technology brings more intelligent, controllable, faster and even operation experiences. First developer of Robotic arm platform treatment device in medical beauty application field. 

Leaflife has obtained various of MDD CE, ROHS, FDA, NMPA，I S O 1 3 4 8 5 and MDSAP more certificates and has got over 40 technical patents as approved National High-tech Enterprise.

       Equipment's sell well all over the                             world
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Exported worldwide over 80 countries                        and regions

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    ISO13485 medical system, MDD, FDA,           CE and Anvisa etc.certificates
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Leaflife is committed to total customer satisfaction by providing consistently high quality products that meet and exceed the expectations of our worldwide customers.
 

Leaflife quality certified ISO 9001:2008, 13485:2012 systems supports its philosophy and mission to continuosly provide the highest quality.

Leaflife Medical products carry the CE marking according to European directive 93/42.

Leaflife Medical products comply with the specific regulations and standards of the countries in which they are offered for sale.

Certificates:

  • EC Certificate Directive93/42/EEC on Medical Device – The design, manufacture of laser therapy devices and non-laser light therapy devices for the treatment of hirsutism. Certification by BSI Group.

  • ISO 13485:2016 & EN ISO 13485:2016 – The design, development, manufacture and distribution of laser therapy devices and non-laser light therapy devices for the treatment of hirsutism. Certification by BSI Group.

  • FDA Approved – Powered Laser Surgical Instrument, Regulation Number 878.4810, Classification Product Code GEX. 510(K) Number:K202980

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