Hiossen, Inc.
MODIFICATION TO: HG III ULTRA WIDE SYSTEM
SKU K093889UPC DZE
In Stock
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IIFDA 510(k) Cleared (K093889)
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Free shipping on orders over $99 · 30-day returns
Hiossen, Inc.
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO: HG III ULTRA WIDE SYSTEM is an FDA 510(k)-cleared medical device (K093889) manufactured by Hiossen, Inc.. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 21, 2010. Regulation: 8.
