Kaylight Corporation is one of 25323 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kaylight Corporation - FDA 510(k) Cleared Devices
Recent clearances: KENKOWAVE INFRARED PAIN TREATMENT SYSTEM
1
Total
1
Cleared
0
Denied
Kaylight Corporation has 1 FDA 510(k) cleared medical devices. Based in Woodbury, US.
Historical record: 1 cleared submissions from 2004 to 2004. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Kaylight Corporation Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Kaylight Corporation
1 devices