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All medical devices are CE marked in accordance with the Medical Devices Directive 93/42/EEC.

We place the highest emphasis on quality and take every measure to keep pace with the changing face of technology. We bring more than 38 years of experience and a passion for perfection to consistently produce products which surpass our customers expectations.


Our Quality Management System is certified to comply with the requirements of ISO 13485:2016/NS-EN ISO 13485:2016 by DNV GL NEMKO PRESAFE AS

EC Certificate No 11174-2017-CE-IND-NA-PS Rev. 0.0 for design, production and final product inspection/testing of Sterile and Non Sterile Disposable Medical Devices issued to us by DNV GL NEMKO PRESAFE AS

FDA. Establishment Registration Number: 3004971305; Owner/Operator Number: 9027362.

Kiato product quality and process parameters are stringently controlled and monitored at each and
every stage of production. Each unit carton is assigned a unique bar coded number, which enables us to track and record process parameters and traceability details of each and every carton.
Image of KIATO surgical blade # 10 edge taken at 2000X using Electron Microscope.
All this has together won us the confidence of our customers and the reputation of a company that is
today a force to be reckoned with in the world of surgical blades.