Medical Device Manufacturer · US , Orlando , FL

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

2 submissions · 2 cleared · Since 2000

Recent clearances: EX-308 EXCIMER LASER FOR PHOTOTHERAPY TREATMENT OF VITILIGO, SURGILIGHT, INC EXCIMER LASER

View 2 510(k) Devices ↓

2

Total

2

Cleared

0

Denied

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

2 devices

1-2 of 2

Cleared Mar 29, 2002

EX-308 EXCIMER LASER FOR PHOTOTHERAPY TREATMENT OF VITILIGO

General & Plastic Surgery · 3d

Cleared Jul 18, 2000

SURGILIGHT, INC EXCIMER LASER

General & Plastic Surgery · 288d