Foreo, Inc.
FAQ (102)
SKU K240616UPC PAY
In Stock
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IIFDA 510(k) Cleared (K240616)
1
Free shipping on orders over $99 · 30-day returns
Foreo, Inc.
Free shipping on orders over $99 · 30-day returns
FAQ (102) is an FDA 510(k)-cleared medical device (K240616) manufactured by Foreo, 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 July 14, 2024. Regulation: 8.
