Dental Handpieces

No FDA recalls on record, checked 10 Oct 2026.

510(k) Number

K760988 ↗

Advisory Committee

Unknown

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

• Zinc Cement

  Class II

  FDA 510(k) K760978 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

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