Dmg USA, Inc.
LUXABITE
SKU K013236UPC ELW
In Stock
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IIFDA 510(k) Cleared (K013236)
1
Free shipping on orders over $99 · 30-day returns
Dmg USA, Inc.
Free shipping on orders over $99 · 30-day returns
LUXABITE is an FDA 510(k)-cleared medical device (K013236) manufactured by Dmg USA, 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 October 16, 2001. Regulation: 8.
