Medical Device Manufacturer · US , Lynnfield , MA

Diomed, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1999

Recent clearances: EVLT KIT AND THE D15PLUS AND D30PLUS DIODE LASERS, EVLT KIT AND D15PLUS AND D30PLUS DIODE, DIOMED 15 PLUS AND DIOMED 30PLUS LASERS

View 5 510(k) Devices ↓

5

Total

5

Cleared

0

Denied

FDA 510(k) Regulatory Record - Diomed, Inc. General & Plastic Surgery ✕

5 devices

1-5 of 5

Cleared Dec 01, 2004

EVLT KIT AND THE D15PLUS AND D30PLUS DIODE LASERS

General & Plastic Surgery · 133d

Cleared Dec 02, 2002

EVLT KIT AND D15PLUS AND D30PLUS DIODE

General & Plastic Surgery · 41d

Cleared Nov 16, 2001

DIOMED 15 PLUS AND DIOMED 30PLUS LASERS

General & Plastic Surgery · 25d

Cleared May 01, 2000

A100 AESTHETIC DIODE LASER

General & Plastic Surgery · 35d

Cleared Feb 26, 1999

General & Plastic Surgery · 53d