Transdermal Cap, Inc. is one of 18426 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Transdermal Cap, Inc. - FDA 510(k) Cleared Devices
Recent clearances: LaserCap Family of Lasers 300, 224, 120 & 80, LaserCap300, LaserCap224, LaserCap120, LaserCap80, LaserCap LC Pro and LC Elite
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.
Regulatory submissions have been managed by Nst Consulting, LLC and Nst Consultants, Inc..
FDA 510(k) Regulatory Record - Transdermal Cap, Inc.
3 devices