FDA Product Code NLQ: Single-use Reprocessed Ultrasonic Surgical Instruments
FDA product code NLQ covers single-use reprocessed ultrasonic surgical instruments cleared for use after validated reprocessing of originally single-use devices.
Ultrasonic surgical instruments are expensive; reprocessing provides a validated, cost-effective alternative that must meet the same safety and functional requirements as the original single-use device, including sterility, functionality, and absence of patient safety risks from reuse.
NLQ devices are reviewed by the FDA General & Plastic Surgery panel.
Leading manufacturers include Sterilmed, Inc., Stryker Sustainability Solutions and Vanguard Medical Concepts, Inc..
27
Total
27
Cleared
171d
Avg days
2001
Since
27 devices
Cleared
Mar 22, 2005
VANGUARD REPROCESSED HAND-ACTIVATED ULTRASONIC SCALPEL
Vanguard Medical Concepts, Inc.
General & Plastic Surgery
111d
Cleared
Jan 23, 2004
MEDISISS REPROCESSED ULTRASONIC SURGICAL INSTRUMENTS
Medisiss
General & Plastic Surgery
332d
Cleared
Nov 07, 2001
REPROCESSED HARMONIC
Sterilmed, Inc.
General & Plastic Surgery
90d