Reprocessed Ultrasonic Curved Shears with Torque Wrench and Grip Assist (FCS9 +… - FCS9

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

510(k) Number

K100537 ↗

FDA Product Code

NLQ

Models / Variants

FCS9

Twblue

Gablue

Device Class

U

Advisory Committee

Unknown

FDA Decision

SESE Substantially Equivalent

• Reprocessed Cs Bi-Diectional Diagnostic Electrophysiology Catheter Open recall

  Class II

  FDA 510(k) K100254 Active Cleared 28 May 2010

• Reprocessed External Fixation Device

  Class II

  FDA 510(k) K061759 Active Cleared 5 Sep 2006

• Reprocessed Diagnostic Ultrasound Catheter

  Class II

  FDA 510(k) K063076 Active Cleared 29 Mar 2007

• Reprocessed Electrosurgical Instrument

  Class II

  FDA 510(k) K110189 Active Cleared 18 Jul 2011

• Reprocessed Trocars

  Class II

  FDA 510(k) K070059 Active Cleared 2 Oct 2007

• Reprocessed Electrophysiology Catheters

  Class II

  FDA 510(k) K090323 Active Cleared 1 Apr 2009

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