Visio-Dispers

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K803227 ↗

FDA Product Code

EBF

Device Class

Class II

Regulation

21 CFR Part 872.3690

Advisory Committee

Dental

FDA Decision

SESE Substantially Equivalent

• Etching Gel

  Class II

  FDA 510(k) K810266 Active Cleared 23 Feb 1981

• Nimetic Polishing Paste

  Class I

  FDA 510(k) K812118 Active Cleared 31 Aug 1981

• Visio-Band

  Class II

  FDA 510(k) K810265 Active Cleared 23 Feb 1981

• Permagum

  Class II

  FDA 510(k) K812116 Active Cleared 31 Aug 1981

• Visio-Seal

  Class II

  FDA 510(k) K811624 Active Cleared 26 Jun 1981

• Permagum Adhesive

  Class II

  FDA 510(k) K812117 Active Cleared 31 Aug 1981

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