Graspers

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K935382 ↗

FDA Product Code

GCJ

Device Class

Class II

Regulation

21 CFR Part 876.1500

Advisory Committee

Gastroenterology, Urology

FDA Decision

SESE Substantially Equivalent

• Tubalgator

  Class II

  FDA 510(k) K113080 Active Cleared 29 Jun 2012

• Insufflation Tubing

  Class II

  FDA 510(k) K925691 Active Cleared 23 Sep 1993

• Insufflator, Laparoscopic

  Class II

  FDA 510(k) K920959 Active Cleared 13 Jul 1992

• Electro-Lube

  Class II

  FDA 510(k) K033880 Active Cleared 10 Mar 2004

• Mectra Trocar

  Class II

  FDA 510(k) K934547 Active Cleared 18 Feb 1994

• Pneumoperitoneum Insufflation Needle

  Class II

  FDA 510(k) K021247 Active Cleared 8 Nov 2002

See all devices from Mectra Labs, Inc. →