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Dental Ventures of America, Inc.

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K000894 C&B RESIN PLUS POWDER/LIQUID, MODELS RETEMP A2, A3, A3.5, CL, RETEMP B2, B3, C2, D3, WH, RETEMP MOEBG2000-05-19 View
510(k) K842377 MS NONPRECIOUS CROWN & BRIDGE ALLOYEJH1984-07-31 View
510(k) K780808 PIEZOMATIC ULTRASONIC SCALER (SYSTEM S)ELC1978-06-22 View
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