Kerr Corporation (Danbury)
KERR OPTIBOND, MODIFICATION
SKU K934690UPC KLE
In Stock
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IIFDA 510(k) Cleared (K934690)
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Free shipping on orders over $99 · 30-day returns
Kerr Corporation (Danbury)
Free shipping on orders over $99 · 30-day returns
KERR OPTIBOND, MODIFICATION is an FDA 510(k)-cleared medical device (K934690) manufactured by Kerr Corporation (Danbury). This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 29, 1993. Regulation: 8.
