We are in the business of helping our customers develop and bring medical devices to market, and then manufacture them in production by using the collective resources of Group Dekko and a bank of highly qualified suppliers.
Offering accredited A2LA Laboratory and Certified UL Test Agency services through the Dekko Technical Center allows us to develop science-based data to support product claims, achieve UL listing for our customers, and support a variety of regulatory related activities.
Important contributions in material selection, method of manufacture, and satisfying compliance and implementation are vital parts of our value added proposition.
At Dekko Medical Devices we have a strong track record of helping our clients eliminate hidden costs, increase inventory turns and profitability while increasing customer service levels. We offer a USA based manufacturing solution with scalable options that may include progressive automation or manufacturing in Mexico. We do not and will not compete with our customers in the marketplace.
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Registered
FDA #9051655
DEKKO MEDICAL DEVICES •
6928 N. 400 E. DOCK 101 •
KENDALLVILLE , IN 46755 USA
TELEPHONE: (800) 829-3101 x 70144 •
FAX: (260) 599-3415 •
EMAIL dekkomedical@dekko.com