Luxalloy 50 (Powder, Tablets, Predosed Capsules)

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K902249 ↗

FDA Product Code

EJJ

Device Class

Class II

Regulation

21 CFR Part 872.3070

Advisory Committee

Dental

FDA Decision

SESE Substantially Equivalent

• Part 872 Degufill H & Degufill M Da

  Class I

  FDA 510(k) K914368 Active Cleared 13 Nov 1991

• Futura One

  Class II

  FDA 510(k) K950187 Active Cleared 24 Mar 1995

• Dentomat 3 Amalgamators

  Class I

  FDA 510(k) K914339 Active Cleared 7 Nov 1991

• Degufill (Tm) Bond

  Class II

  FDA 510(k) K902744 Active Cleared 15 Aug 1990

• Degussa Stopfgold (Degussa Direct-Filling Gold)

  Class II

  FDA 510(k) K902387 Active Cleared 28 Jun 1990

• Palliag Nf IV

  Class II

  FDA 510(k) K951789 Active Cleared 14 Jun 1995

See all devices from Degussa AG →