Vitapan Acrylic Denture Teeth

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

510(k) Number

K914476 ↗

FDA Product Code

ELM

Device Class

Class II

Regulation

21 CFR Part 872.3590

Advisory Committee

Dental

FDA Decision

SESE Substantially Equivalent

• Vita Titanium Porcelain

  Class II

  FDA 510(k) K982664 Active Cleared 2 Aug 1998

• Vita Response

  Class II

  FDA 510(k) K000597 Active Cleared 17 May 2000

• V.R.S. Denture Resin Material

  Class II

  FDA 510(k) K962333 Active Cleared 7 Aug 1996

• In-Ceram Spinell

  Class II

  FDA 510(k) K951183 Active Cleared 2 May 1995

• Vita Vm 7, Model NX77 Xxxx, NX78XXXX, NX79 Xxxx; Vita Vm 8, Model VX60 Xxxx, VX61 Xxxx, VX62 Xxxx; Vita Vm 9, Model NX98

  Class II

  FDA 510(k) K060441 Active Cleared 27 Apr 2006

• Vita Pm 7 (20 Gram Bottles), Vita Pm 7 (50 Gram Bottles)

  Class II

  FDA 510(k) K050362 Active Cleared 15 Mar 2005

See all devices from Vident →