Trophy Skin, Inc. is one of 18426 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Trophy Skin, Inc. - FDA 510(k) Cleared Devices
Recent clearances: RejuvatoneMD, HairMD, REJUVALITE MD
3
Total
3
Cleared
0
Denied
Trophy Skin, Inc. has 3 FDA 510(k) cleared medical devices. Based in Coralville, US.
Historical record: 3 cleared submissions from 2014 to 2016. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Trophy Skin, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Nst Consulting, Inc. and Aegis Regulatory, Inc..
FDA 510(k) Regulatory Record - Trophy Skin, Inc.
3 devices