March 2017
Company "continuous immunoassay analyzer WIZ-A202" won the Fujian Medical Device Registration Certificate.
February 2017
Companies in the country's share transfer system for SMEs (the new board) listed.
March 2016
Obtained  three kinds of in vitro diagnostic reagents approved by the State Food  and Drug Administration a total of eight product registration  certificate.
February 2016
The company as a whole changed to a limited liability company, changed its name to "Xiamen is Biotechnology Co., Ltd.".
January 2016      
Obtained by the SGS ISO13485, ISO9001 quality system certification.
October 2015    
 Access to "high-tech enterprise certificate."
September 2015
Made in Fujian Province Food and Drug Administration approved the second category of in vitro diagnostic reagents a total of seven products. Of the certificate of registration, including "Calprotectin test kit (colloidal gold method)" products for the domestic initiative.
October 2014 
The type of company changed from a domestic-funded enterprise to a Sino-foreign joint venture.
September 2014 
Through the SFDA in vitro diagnostic reagents quality management system assessment.
April 2014 
Access to Food and Drug Administration certification "medical equipment manufacturing enterprises permit."
July 2013
Founded.