Medical Device Manufacturer · US , Payton , CO

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

2 submissions · 2 cleared · Since 2000

Total

Cleared

Denied

Light Force Therapy, Inc. has 2 FDA 510(k) cleared medical devices. Based in Payton, US.

Historical record: 2 cleared submissions from 2000 to 2002. Primary specialty: Physical Medicine.

Browse the FDA 510(k) cleared devices submitted by Light Force Therapy, Inc. Filter by specialty or product code using the sidebar.

Light Force Therapy, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

2 devices

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