Dio Corporation
DIO UF HSA INTERNAL SUB-MERGED IMPLANT SYSTEM
SKU K122519UPC DZE
In Stock
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IIFDA 510(k) Cleared (K122519)
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Free shipping on orders over $99 · 30-day returns
Dio Corporation
Free shipping on orders over $99 · 30-day returns
DIO UF HSA INTERNAL SUB-MERGED IMPLANT SYSTEM is an FDA 510(k)-cleared medical device (K122519) manufactured by Dio Corporation. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 20, 2013. Regulation: 8.
