Medical Device Manufacturer · US , Payton , CO

Light Force Therapy, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2000

Recent clearances: ACUBEAM, SUPER NOVA, DIO, SUPER NOVA, ACUBEAM

View 2 510(k) Devices ↓

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Light Force Therapy, Inc. Physical Medicine ✕

2 devices

1-2 of 2

Cleared Dec 11, 2002

ACUBEAM, SUPER NOVA, DIO

Physical Medicine · 103d

Cleared Oct 27, 2000

SUPER NOVA, ACUBEAM

Physical Medicine · 199d