Dentrol Liquid Denture Adhesive

No FDA recalls on record, checked 11 Oct 2026.

510(k) Number

K780849 ↗

Advisory Committee

Unknown

FDA Decision

SESE Substantially Equivalent

• Vision Prophy Paste Without Fluoride

  Class I

  FDA 510(k) K933893 Active Cleared 16 Nov 1993

• Vision Prophy Paste with Fluoride

  Class I

  FDA 510(k) K935925 Active Cleared 26 Jan 1994

• Sensodyne Sealant Dentin Conditioning System

  Class II

  FDA 510(k) K884533 Active Cleared 12 Apr 1989

• Duo Two Layer Denture Cleanser

  Class I

  FDA 510(k) K791064 Active Cleared 9 Oct 1979

• Py-Co-Prox Tm Dental Brush

  Class I

  FDA 510(k) K800831 Active Cleared 8 May 1980

• Proficient(Tm) Prophylaxis Angle

  Class I

  FDA 510(k) K881974 Active Cleared 25 Jul 1988

See all devices from Block Drug Company, Inc. →