Medical Device Manufacturer · US , Woodbury , CT

Kaylight Corporation - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2004

Recent clearances: KENKOWAVE INFRARED PAIN TREATMENT SYSTEM

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Kaylight Corporation Physical Medicine ✕

1 devices

1-1 of 1

Cleared Mar 02, 2004

KENKOWAVE INFRARED PAIN TREATMENT SYSTEM

Physical Medicine · 111d

Data Source

Sourced from the FDA 510(k) public files . 176,583 total devices indexed.

Last updated: Oct 11, 2026