Surgi-Brush

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

510(k) Number

K896085 ↗

FDA Product Code

GEC

Device Class

Class I

Regulation

21 CFR Part 878.4800

Advisory Committee

General, Plastic Surgery

FDA Decision

SESE Substantially Equivalent

• Spectrum II, Spectrum Plus, and Spectrum Max-Sd

  Class II

  FDA 510(k) K965187 Active Cleared 1 Aug 1997

• Sparta Hydrogel Wound Dressing

  Unclassified

  FDA 510(k) K945313 Active Cleared 12 Jan 1995

• Vesseloops

  Class I

  FDA 510(k) K905240 Active Cleared 6 Feb 1991

• Sparta Wet Dressing, Sodium Chloride

  Unclassified

  FDA 510(k) K922729 Active Cleared 23 Nov 1992

• David Simmonds Anesthesia Extension Tubes

  Class II

  FDA 510(k) K905384 Active Cleared 22 Mar 1991

• Microspears

  Class II

  FDA 510(k) K896084 Active Cleared 2 Nov 1989