Duo Two Layer Denture Cleanser

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K791064 ↗

FDA Product Code

EFT

Device Class

Class I

Regulation

21 CFR Part 872.3520

Advisory Committee

Dental

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

• 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

• Dentrol Liquid Denture Adhesive

  Not classified

  FDA 510(k) K780849 Active Cleared 31 Jul 1978

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