Transdermal Cap, Inc. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Transdermal Cap, Inc. has 3 FDA 510(k) cleared medical devices. Based in Cleveland, US.
Last cleared in 2021. Active since 2015. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Transdermal Cap, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Nst Consultants, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Transdermal Cap, Inc.
3 devices