DW217 #18 Crown/Bridge & DW218 #24 Ceramic Alloys

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K860439 ↗

FDA Product Code

EJS

Device Class

Class II

Regulation

21 CFR Part 872.3060

Advisory Committee

Dental

FDA Decision

SESE Substantially Equivalent

• Dura-Vac

  Not classified

  FDA 510(k) K770545 Active Cleared 24 Mar 1977

• Renaissance

  Class II

  FDA 510(k) K844395 Active Cleared 9 Jan 1985

• Will-Ceram Y-2

  Class II

  FDA 510(k) K760122 Active Cleared 16 Jul 1976

• Disposable Articulator

  Class I

  FDA 510(k) K801342 Active Cleared 8 Jul 1980

• A Thenium

  Class II

  FDA 510(k) K821510 Active Cleared 9 Jun 1982

• Gold, 24 Karat Casting

  Class II

  FDA 510(k) K781788 Active Cleared 28 Dec 1978

See all devices from Williams Gold Refining Co., Inc. →