Plastikon Industries is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Plastikon Industries - FDA 510(k) Cleared Devices
Recent clearances: ICU Health Surgical Mask
1
Total
1
Cleared
0
Denied
Plastikon Industries has 1 FDA 510(k) cleared medical devices. Based in Hayward, US.
Last cleared in 2021. Active since 2021. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Plastikon Industries Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hantel Technologies, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Plastikon Industries
1 devices