Depilase Yag Lase Plus Laser System

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

510(k) Number

K030506 ↗

FDA Product Code

GEX

FDA applicant

Depilase Group , Ltd.

Device Class

Class II

Regulation

21 CFR Part 878.4810

Advisory Committee

General, Plastic Surgery

FDA Decision

SESE Substantially Equivalent

• Depilase Twin YAG Laser System

  Class II

  FDA 510(k) K030510 Active Cleared 14 May 2003

• Depilase Trio Lase Laser System

  Class II

  FDA 510(k) K030508 Active Cleared 20 May 2003

• Depilase Yaglase Nd:yag Laser System and Accessories

  Class II

  FDA 510(k) K001990 Active Cleared 23 Oct 2000

• Depilase Twin Lase Laser System

  Class II

  FDA 510(k) K020412 Active Cleared 22 Feb 2002

• Depilase Yag Lase Plus Laser System

  Class II

  FDA 510(k) K020463 Active Cleared 27 Feb 2002

• Depilase Twin Yag Laser System

  Class II

  FDA 510(k) K020697 Active Cleared 12 Apr 2002