Tria Beauty, Inc. is one of 4783 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tria Beauty, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Tria Beauty, Inc. has 5 FDA 510(k) cleared medical devices. Based in Washington D.C., US.
Historical record: 5 cleared submissions from 2010 to 2016. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Tria Beauty, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Tria Beauty, Inc.
5 devices
Cleared
Jun 15, 2016
Tria Sapphire
General & Plastic Surgery
83d
Cleared
Dec 30, 2014
TRIA FANP
General & Plastic Surgery
173d
Cleared
Oct 25, 2013
TRIA FAN SYSTEM
General & Plastic Surgery
245d
Cleared
Sep 13, 2012
TRIA LASER HAIR REMOVAL SYSTEM
General & Plastic Surgery
188d
Cleared
Jan 05, 2010
TRIA ACNE TREATMENT SYSTEM, MODEL ATS-1 OTC
General & Plastic Surgery
333d