Dioscan

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K990014 ↗

FDA Product Code

GEX

Device Class

Class II

Regulation

21 CFR Part 878.4810

Advisory Committee

General, Plastic Surgery

FDA Decision

SESE Substantially Equivalent

• Diomed 15 Diode Laser

  Class II

  FDA 510(k) K012398 Active Cleared 22 Jan 2002

• A100 Aesthetic Diode Laser

  Class II

  FDA 510(k) K000982 Active Cleared 1 May 2000

• Diomed 25 25W Surgical Diode Laser

  Class II

  FDA 510(k) K931776 Active Cleared 19 Oct 1993

• Diomed Delta 25

  Class II

  FDA 510(k) K063828 Active Cleared 25 Jan 2007

• Diomed 25 Surgical Diode Laser, Gynecology Applic

  Class II

  FDA 510(k) K914519 Active Cleared 16 Sep 1993

• Diomed 25 Surgical Diode Laser, Urology Applicat

  Class II

  FDA 510(k) K914520 Active Cleared 22 Jan 1993

See all devices from Diomed, Inc. →