Hiossen, Inc.
ET Hybrid Abutment
SKU K162390UPC NHA
In Stock
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IIFDA 510(k) Cleared (K162390)
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Free shipping on orders over $99 · 30-day returns
Hiossen, Inc.
Free shipping on orders over $99 · 30-day returns
ET Hybrid Abutment is an FDA 510(k)-cleared medical device (K162390) 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 January 29, 2017. Regulation: 8.
