Zinc Cement

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K760978 ↗

FDA Product Code

EMA

Device Class

Class II

Regulation

21 CFR Part 872.3275

Advisory Committee

Dental

FDA Decision

SESE Substantially Equivalent

• Hand Instruments

  Class I

  FDA 510(k) K760985 Active Cleared 15 Nov 1976

• Alginate Impression Material

  Class II

  FDA 510(k) K760981 Active Cleared 15 Nov 1976

• Dental Handpieces

  Not classified

  FDA 510(k) K760988 Active Cleared 15 Nov 1976

• Dental Varnish

  Class II

  FDA 510(k) K760982 Active Cleared 15 Nov 1976

• Orthodontic Instruments

  Class I

  FDA 510(k) K760984 Active Cleared 15 Nov 1976

• Dental Alloy

  Class II

  FDA 510(k) K760980 Active Cleared 15 Nov 1976

See all devices from Adp Intl., Inc. →