Videoscope W/Irrigation Sheath

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K954016 ↗

FDA Product Code

HRX

Device Class

Class II

Regulation

21 CFR Part 888.1100

Advisory Committee

Orthopedic

FDA Decision

SN

• Cervical Self-Retaining Retractor

  Class II

  FDA 510(k) K935529 Active Cleared 22 Mar 1994

• Sternum Spreader and Mitral Valve Retractor

  Class I

  FDA 510(k) K881157 Active Cleared 6 Apr 1988

• Percutaneous Discectomy Cannula System

  Class II

  FDA 510(k) K954014 Active Cleared 6 Nov 1995

• Sternum Spreader, Pediatric

  Class I

  FDA 510(k) K880998 Active Cleared 21 Mar 1988

• Reusable Endoscopic Scissors, Grasper-Monopolar

  Class II

  FDA 510(k) K926583 Active Cleared 6 Aug 1993

• Non-Absorbing Sternatomy Monofilament Suture

  Class II

  FDA 510(k) K002755 Active Cleared 4 Dec 2000

See all devices from T. Korossurgical Instruments Corp. →