Dexide Laparoscopic Kits

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K924117 ↗

FDA Product Code

KDD

Device Class

Class I

Regulation

21 CFR Part 878.4800

Advisory Committee

General, Plastic Surgery

FDA Decision

SESK Substantially Equivalent — Kit

• Monoscopy Brand 5mm Lock Trocar Sleeve, Modified

  Class II

  FDA 510(k) K912980 Active Cleared 26 Jul 1991

• Multaport Cannula Reducer and Accessories

  Class II

  FDA 510(k) K981941 Active Cleared 29 Jul 1998

• Multapump Disposable Pump Head and Accessories

  Class II

  FDA 510(k) K981940 Active Cleared 25 Sep 1998

• Dexide Insufflation Tubing with Filter

  Class II

  FDA 510(k) K944509 Active Cleared 7 Feb 1995

• Distendable Palpation Probe

  Class II

  FDA 510(k) K912343 Active Cleared 18 Jun 1991

• Dexide Laparoscopic Accessories

  Class II

  FDA 510(k) K923845 Active Cleared 25 Nov 1992

See all devices from Dexide, Inc. →