Beach Anesthetic Syringe Cartr. Type

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K821782 ↗

FDA Product Code

EJI

Device Class

Class II

Regulation

21 CFR Part 872.6770

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 High Volume Evacuation Handpie

  Class I

  FDA 510(k) K801682 Active Cleared 4 Aug 1980

• 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

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