Satelec - Acteon Group
I-ENDO DUAL
SKU K111623UPC EBW
In Stock
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IFDA 510(k) Cleared (K111623)
1
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Satelec - Acteon Group
Free shipping on orders over $99 · 30-day returns
I-ENDO DUAL is an FDA 510(k)-cleared medical device (K111623) manufactured by Satelec - Acteon Group. This device is classified under the Dental specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on January 9, 2012. Regulation: 8.
