Endo-Lase Cd-100 CO2 Laser for Dermatology

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K853877 ↗

FDA Product Code

GEX

Device Class

Class II

Regulation

21 CFR Part 878.4810

Advisory Committee

General, Plastic Surgery

FDA Decision

SESE Substantially Equivalent

• Endo-Lase Cd-100 CO2 Laser for Otorhinolaryngology

  Class II

  FDA 510(k) K853875 Active Cleared 9 Jan 1986

• Flexible Liquid Light Guide

  Class II

  FDA 510(k) K834487 Active Cleared 21 Feb 1984

• Utilization of Nd:yag Laser for Treatment Rectal P

  Class II

  FDA 510(k) K851527 Active Cleared 17 May 1985

• Infrared Coagulator

  Class II

  FDA 510(k) K842810 Active Cleared 18 Oct 1984

• Nd. Yag Laser for Endobronchial Obstruc

  Not classified

  FDA 510(k) K843228 Active Cleared 4 Sep 1984

• Medilas 2 Nd:yag Laser Surgery System

  Class II

  FDA 510(k) K855093 Active Cleared 21 Feb 1986

See all devices from Endo Lase, Inc. →