Zuko, Inc. is one of 18413 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Zuko, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Acne Light Therapy Wand
1
Total
1
Cleared
0
Denied
Zuko, Inc. has 1 FDA 510(k) cleared medical devices. Based in Wayne, US.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Zuko, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Texas Applied Biomedical Services (T.A.B.S.) as regulatory consultant.
FDA 510(k) Regulatory Record - Zuko, Inc.
1 devices