Coherent Versapulse Aesthetic Surgical Lasers

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K960032 ↗

FDA Product Code

GEX

Device Class

Class II

Regulation

21 CFR Part 878.4810

Advisory Committee

General, Plastic Surgery

FDA Decision

SESE Substantially Equivalent

• Lds - Laser Delivery System

  Class II

  FDA 510(k) K862568 Active Cleared 7 Oct 1986

• Coherent Xa-30 CO2 Surgical Laser

  Class II

  FDA 510(k) K873963 Active Cleared 19 Oct 1987

• Model 5001 Micromanipulator for Use W/Tf-25 CO2

  Class II

  FDA 510(k) K873246 Active Cleared 10 Nov 1987

• Versapulse(Tm) Twopointone/Xe Holmium Surg Lasers

  Class II

  FDA 510(k) K914991 Active Cleared 6 May 1992

• Laser Indirect Ophthalmoscope (Lio)

  Class II

  FDA 510(k) K885196 Active Cleared 11 Jan 1989

• Model 920 Argon/Dye Laser-for Dermatological/Use

  Class II

  FDA 510(k) K852860 Active Cleared 7 Oct 1985

See all devices from Coherent Medical Group →