Candela Corporation
Profound Matrix
SKU K211217UPC GEI
In Stock
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IIFDA 510(k) Cleared (K211217)
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Free shipping on orders over $99 · 30-day returns
Candela Corporation
Free shipping on orders over $99 · 30-day returns
Profound Matrix is an FDA 510(k)-cleared medical device (K211217) manufactured by Candela Corporation. 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 December 15, 2021. Regulation: 8.
