Voco GmbH
REGISTRADO X-TRA
SKU K022066UPC ELW
In Stock
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IIFDA 510(k) Cleared (K022066)
1
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Voco GmbH
Free shipping on orders over $99 · 30-day returns
REGISTRADO X-TRA is an FDA 510(k)-cleared medical device (K022066) manufactured by Voco GmbH. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 13, 2002. Regulation: 8.
