Dexide Laparoscopic Accessories

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K923845 ↗

FDA Product Code

GEI

Device Class

Class II

Regulation

21 CFR Part 878.4400

Advisory Committee

General, Plastic Surgery

FDA Decision

SESE Substantially Equivalent

• 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 Disposable Prep Sponge

  Class I

  FDA 510(k) K791166 Active Cleared 10 Jul 1979

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