Dental Ventures of America, Inc.
C&B RESIN PLUS POWDER/LIQUID, MODELS RETEMP A2, A3, A3.5, CL, RETEMP B2, B3, C2, D3, WH, RETEMP MO
SKU K000894UPC EBG
In Stock
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IIFDA 510(k) Cleared (K000894)
1
Free shipping on orders over $99 · 30-day returns
Dental Ventures of America, Inc.
Free shipping on orders over $99 · 30-day returns
C&B RESIN PLUS POWDER/LIQUID, MODELS RETEMP A2, A3, A3.5, CL, RETEMP B2, B3, C2, D3, WH, RETEMP MO is an FDA 510(k)-cleared medical device (K000894) manufactured by Dental Ventures of America, Inc.. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 18, 2000. Regulation: 8.
