Denali Corporation
Resolve 2.0
SKU K152322UPC PME
In Stock
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IIFDA 510(k) Cleared (K152322)
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Free shipping on orders over $99 · 30-day returns
Denali Corporation
Free shipping on orders over $99 · 30-day returns
Resolve 2.0 is an FDA 510(k)-cleared medical device (K152322) manufactured by Denali 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 December 15, 2015. Regulation: 8.
