Gdc-1433 a Casting Alloy

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K850102 ↗

FDA Product Code

EJS

Device Class

Class II

Regulation

21 CFR Part 872.3060

Advisory Committee

Dental

FDA Decision

SESE Substantially Equivalent

• Neydium Npflux (for Soldering)

  Not classified

  FDA 510(k) K770159 Active Cleared 31 Jan 1977

• Gdc-3338, Dental Solder Alloy

  Class II

  FDA 510(k) K920887 Active Cleared 19 Mar 1992

• Ultima Lite

  Class II

  FDA 510(k) K890568 Active Cleared 9 Mar 1989

• Gdc 1448 Development Name

  Class II

  FDA 510(k) K833596 Active Cleared 29 Dec 1983

• Gdc-685

  Class II

  FDA 510(k) K790641 Active Cleared 1 May 1979

• Tempo

  Class II

  FDA 510(k) K792274 Active Cleared 30 Nov 1979

See all devices from Deringer-Ney, Inc. →