Spaceline High Volume Evacuation Handpie

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K801682 ↗

FDA Product Code

EHZ

Device Class

Class I

Regulation

21 CFR Part 872.6640

Advisory Committee

Dental

FDA Decision

SESE Substantially Equivalent

• Beach Deriosteal Elevator, #2 Straight

  Class I

  FDA 510(k) K821788 Active Cleared 6 Jul 1982

• Spaceline Dental Chair-Unit

  Class I

  FDA 510(k) K801685 Active Cleared 4 Aug 1980

• Beach Forcep No. 150 and No. 151

  Class I

  FDA 510(k) K821781 Active Cleared 2 Jul 1982

• Beach Dressing Plier

  Class I

  FDA 510(k) K821778 Active Cleared 6 Jul 1982

• Beach Amalgam Carver

  Class I

  FDA 510(k) K821785 Active Cleared 6 Jul 1982

• J. Morita Flex M-3 Torx Hardpiece

  Class I

  FDA 510(k) K821739 Active Cleared 25 Jun 1982

See all devices from Pacific Dental Corp. →