Diamond Diagnostics is the global leader and premier supplier of high quality refurbished clinical laboratory equipment. Diamond is the only refurbisher carrying US FDA registration along with certifications in both ISO 9001:2015 and ISO 13485:2016. Diamond has sold over 20,000 systems in over 100 countries earning us the status of the largest Clinical Laboratory refurbishing operation in the world. All instruments refurbished by Diamond Diagnostics undergo our trademark and rigorous Down-To-Frame® refurbishment process providing medical institutions with a reliable and cost-effective alternative to new instrumentation.
Our line of instrumentation includes over 350 manufacturers and models of Blood Gas, Electrolyte, Chemistry, Immunology, Hematology, Coagulation, and Urinalysis systems from all the leading Original Equipment Manufacturers
Diamond Diagnostics offers refurbished for the following categories:
The Diasorin Liaison XL Immunology Analyzer, provided by Diasorin Related Products Service Options Consumables Quality Controls Service Parts
The Elan ATAC 8000 wISE Chemistry Analyzer, provided by ELITech Group Related Products Service Options Consumables Quality Controls Service Parts
The Elitech Envoy 500+ w/ISE Chemistry Analyzer, provided by ELITech Group Related Products Service Options Consumables Quality Controls Service Parts
The Horiba Micros 60CS Hematology Analyzer, provided by Horiba Medical Related Products Service Options Consumables Quality Controls Service Parts
The Horiba Micros 60ES Hematology Analyzer, provided by Horiba Medical Related Products Service Options Consumables Quality Controls Service Parts
Corporate Headquarters (USA)
Diamond Diagnostics Inc.
333 Fiske Street
Holliston, MA 01746-2048
Tel: +1 508.429.0450
Distribution Center (EU)
Diamond Diagnostics Kft.
1044 Budapest, Hungary
Óradna Street 6
Tel: +36 (1) 787 2222
Diamond Diagnostics Inc. is registered with the United States Food and Drug Administration as an Initial Importer Manufacturer and Contract Manufacturer. Establishment registration and device listing can be found under ID: 3003030793.
Diamond has been registered with the Food and Drug Administration since 2001 and regulated by its cGMP system requirements.
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.
The names and logos of manufacturers, their instruments, and their products referred to herein may be protected by trademark or other law, and are used herein solely for purpose of reference. Products are available for international distribution only unless otherwise indicated. Diamond Diagnostics expressly disclaims any affiliation with products it does not manufacture, as well as sponsorship by other manufacturers. For current regulatory status on products within this website, please contact your sales representative. Prices and Information shown are for reference only and may change without notice. SmartLyte®, ProLyte®, CareLyte®, and Down-To-Frame® Refurbishing are Registered Trademarks of Diamond Diagnostics®.