Improved Dental Chair

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K920016 ↗

FDA Product Code

KLC

Device Class

Class I

Regulation

21 CFR Part 872.6250

Advisory Committee

Dental

FDA Decision

SESE Substantially Equivalent

• Evacuator, Oral Cavity

  Class I

  FDA 510(k) K932824 Active Cleared 28 Sep 1993

• Improved Dental Operating Light

  Class I

  FDA 510(k) K920017 Active Cleared 2 Mar 1992

• Panoramic X-Ray, Dental

  Class II

  FDA 510(k) K780469 Active Cleared 10 Apr 1978

• Accessory to Improved Dental Operating Light

  Class I

  FDA 510(k) K925629 Active Cleared 23 Nov 1993

• Autochuck Attachment

  Class I

  FDA 510(k) K874294 Active Cleared 29 Dec 1987

• AS3000 Operative Dental Unit (Delivery System)

  Class I

  FDA 510(k) K931204 Active Cleared 8 Jul 1993