Bellus Medical, LLC
SkinPen Precision System
SKU DEN160029UPC QAI
In Stock
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IIFDA 510(k) Cleared (DEN160029)
1
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Bellus Medical, LLC
Free shipping on orders over $99 · 30-day returns
SkinPen Precision System is an FDA 510(k)-cleared medical device (DEN160029) manufactured by Bellus Medical, LLC. 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 February 28, 2018. Regulation: 8.
