Diamond Diagnostics Inc.

Diamond prides itself on developing and consistently manufacturing products in conformance to the highest quality standards while meeting customer needs. We strive to meet and beat your quality expectations and will continue to improve the quality and value of our final product. Diamond has been registered with the United States Food and Drug Administration since 2001 and regulated by its cGMP system requirements. Since 2006, Diamond has been certified to both ISO 9001:2015 and ISO 13485:2016 standards and has successfully maintained since. All products manufactured by Diamond carry the necessary FDA clearance and comply to the European Union IVD Directive. Every department and function in our company is standardized, controlled and routinely audited. Diamond offers options to either recycle, exchange or complete contract refurbishment of instrumentation from anywhere in the globe.