Vega Dental Operating Light

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K854646 ↗

FDA Product Code

EBA

Device Class

Class I

Regulation

21 CFR Part 872.4630

Advisory Committee

Dental

FDA Decision

SESE Substantially Equivalent

• Gold Air, Gold Light

  Class I

  FDA 510(k) K854645 Active Cleared 12 Mar 1986

• Polo Dental Unit

  Class I

  FDA 510(k) K854647 Active Cleared 5 Jun 1986

• Skema (Dental Unit)

  Class I

  FDA 510(k) K880475 Active Cleared 23 Sep 1988

• Manta Dental Chair

  Class I

  FDA 510(k) K854644 Active Cleared 23 Jan 1986

• Area (Dental Chair)

  Class I

  FDA 510(k) K880474 Active Cleared 23 Sep 1988

• X-Range 65

  Class II

  FDA 510(k) K854741 Active Cleared 6 Mar 1986

See all devices from Alpine Dental Equipment Co. →