Thermage, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Thermage, Inc. - FDA 510(k) Cleared Devices
18
Total
18
Cleared
0
Denied
Thermage, Inc. has 18 FDA 510(k) cleared general & plastic surgery devices. Based in Hayward, US.
Historical record: 18 cleared submissions from 2000 to 2010.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Thermage, Inc.
18 devices
Cleared
Sep 08, 2010
FRAXEL RE:STORE DUAL LASER SYSTEM: MODEL, MC-SYS-SR1500-D-US
General & Plastic Surgery
99d
Cleared
Jan 18, 2008
MODIFICATION TO THERMAGE THERMACOOL SYSTEM
General & Plastic Surgery
106d
Cleared
Jun 12, 2007
THERMAGE THERMACOOL SYSTEM
General & Plastic Surgery
601d
Cleared
Oct 12, 2006
THERMASSAGE
General & Plastic Surgery
184d
Cleared
Dec 13, 2005
MODIFICATION TO THERMAGE THERMACOOL SYSTEM
General & Plastic Surgery
11d
Cleared
Oct 20, 2005
THERMAGE THERMACOOL SKIN MARKETING
General & Plastic Surgery
17d
Cleared
Jul 19, 2005
THERMAGE THERMACOOL COUPLING FLUID
General & Plastic Surgery
22d
Cleared
Jan 14, 2005
THERMAGE THERMACOOL SYSTEM
General & Plastic Surgery
35d
Cleared
Jun 21, 2004
THERMAGE THERMACOOL SYSTEM
General & Plastic Surgery
151d
Cleared
Feb 04, 2004
THERMAGE THERMACOOL SYSTEM
General & Plastic Surgery
47d
Cleared
Aug 01, 2003
MODIFICATION TO THERMACOOL TC SYSTEM
General & Plastic Surgery
25d
Cleared
May 22, 2003
THERMACOOL TC SYSTEM
General & Plastic Surgery
50d