American Dental Technologies, Inc.
DIOLASE 980 D LASER SYSTEM
SKU K023547UPC GEX
In Stock
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IIFDA 510(k) Cleared (K023547)
1
Free shipping on orders over $99 · 30-day returns
American Dental Technologies, Inc.
Free shipping on orders over $99 · 30-day returns
DIOLASE 980 D LASER SYSTEM is an FDA 510(k)-cleared medical device (K023547) manufactured by American Dental Technologies, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 14, 2003. Regulation: 8.
