Corrected-V.P.S.

• • Terminated Z-1146-2012 FDA Unclassified (pre-2012) ·initiated 4 Nov 2010

  Pentron Clinical is voluntarily recalling the following lot of mislabeled Correct VPS Medium Body Tubes. It was discovered that the individual tubes inside the Correct VPS Medium Body Tube boxes are missing the lot/expiration date sticker.

510(k) Number

K914178 ↗

FDA Product Code

ELW

Device Class

Class II

Regulation

21 CFR Part 872.3660

Advisory Committee

Dental

FDA Decision

SESE Substantially Equivalent

• KB58-Kf

  Class II

  FDA 510(k) K922958 Active Cleared 26 Feb 1993

• Prop. Conquest C&B Vlc Glaze/Sealant

  Class II

  FDA 510(k) K953381 Active Cleared 27 Sep 1995

• Crown and Bridge Dental Restorative Composite Syst

  Class II

  FDA 510(k) K894644 Active Cleared 20 Oct 1989

• Orosphere Hcdp

  Class II

  FDA 510(k) K890681 Active Cleared 2 May 1989

• Conquest Crystal

  Class II

  FDA 510(k) K932154 Active Cleared 15 Sep 1993

• Bond-It Dual Cure Activator

  Class II

  FDA 510(k) K953859 Active Cleared 7 Sep 1995

See all devices from Jeneric/Pentron, Inc. →