Reliant Technologies, Inc. is one of 5539 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Reliant Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: FRAXEL RE:PAIR (FRAXEL III SR) LASER SYSTEM AND ACCESSORIES, FRAXEL III SR LASER SYSTEM AND ACCESSORIES, RELIANT TECHNOLOGIES C300 CHILLER SYSTEM AND ACCESSORIES
19
Total
19
Cleared
0
Denied
Reliant Technologies, Inc. has 19 FDA 510(k) cleared general & plastic surgery devices. Based in Foster City, US.
Historical record: 19 cleared submissions from 1994 to 2008.
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 - Reliant Technologies, Inc.
19 devices
Cleared
Jul 01, 2008
FRAXEL RE:PAIR (FRAXEL III SR) LASER SYSTEM AND ACCESSORIES
General & Plastic Surgery
90d
Cleared
Nov 02, 2007
FRAXEL III SR LASER SYSTEM AND ACCESSORIES
General & Plastic Surgery
203d
Cleared
Oct 09, 2007
RELIANT TECHNOLOGIES C300 CHILLER SYSTEM AND ACCESSORIES
General & Plastic Surgery
117d
Cleared
May 17, 2007
FRALEX SR 1500 LASER SYSTEM (FRALEX II SR LASER SYSTEM)
General & Plastic Surgery
108d
Cleared
Apr 27, 2007
FRAXEL III SR LASER SYSTEM AND ACCESSORIES
General & Plastic Surgery
207d
Cleared
Apr 27, 2007
FRAXEL IV SR LASER SYSTEM
General & Plastic Surgery
126d
Cleared
Jan 31, 2007
FRAXEL II SR LASER SYSTEM
General & Plastic Surgery
176d
Cleared
Mar 29, 2006
FRAXEL II SR LASER SYSTEM AND ACCESSORIES
General & Plastic Surgery
50d
Cleared
Mar 20, 2006
FRAXEL SR LASER SYSTEM
General & Plastic Surgery
143d
Cleared
Jul 05, 2005
FRAXEL SR LASER SYSTEM
General & Plastic Surgery
95d
Cleared
Mar 10, 2005
RELIANT LASER II SYSTEM AND ACCESSORIES
General & Plastic Surgery
196d
Cleared
Jun 15, 2004
RELIANT LASER SYSTEM II
General & Plastic Surgery
98d