Cutera, Inc.
truSculpt iD
SKU K221407UPC GEI
In Stock
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IIFDA 510(k) Cleared (K221407)
1
Free shipping on orders over $99 · 30-day returns
Cutera, Inc.
Free shipping on orders over $99 · 30-day returns
truSculpt iD is an FDA 510(k)-cleared medical device (K221407) manufactured by Cutera, 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 12, 2022. Regulation: 8.
