New Star Lasers, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
New Star Lasers, Inc. - FDA 510(k) Cleared Devices
29
Total
29
Cleared
0
Denied
New Star Lasers, Inc. has 29 FDA 510(k) cleared general & plastic surgery devices. Based in Auburn, US.
Historical record: 29 cleared submissions from 1995 to 2014.
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 - New Star Lasers, Inc.
29 devices
Cleared
Oct 31, 2014
NS3000 Holmium Laser System
General & Plastic Surgery
74d
Cleared
Mar 21, 2014
NS 2500 HOLMIUM LASER SYSTEM
General & Plastic Surgery
213d
Cleared
Nov 01, 2011
COOLTOUCH
General & Plastic Surgery
351d
Cleared
Sep 13, 2010
COOLTOUCH MODEL CT3PZ, COOLTOUCH CT3 PLUS COOLBREEZE
General & Plastic Surgery
80d
Cleared
Dec 11, 2009
COOLTOUCH VARIA ND:YAG LASER SYSTEM
General & Plastic Surgery
77d
Cleared
Mar 27, 2009
COOLTOUCH THERMAL SENSING HANDPIECE ACCESSORY
General & Plastic Surgery
37d
Cleared
Jun 20, 2008
MODIFICATION TO COOLTOUCH, MODELS LC225 AND COOLLIPO
General & Plastic Surgery
10d
Cleared
Apr 10, 2008
COOLTOUCH MODELS LC215 AND COOLLIPO
General & Plastic Surgery
78d
Cleared
Jan 02, 2008
COOLTOUCH MODELS NS 160 AND LC215 COOLIPO
General & Plastic Surgery
97d
Cleared
Oct 03, 2007
COOLTOUCH, MODEL LC215,COOLLIPO
General & Plastic Surgery
35d
Cleared
Sep 25, 2006
COOLTOUCH, MODEL CTEV
General & Plastic Surgery
108d
Cleared
Sep 25, 2006
COOL TOUCH, MODELS CT3S, CTEV, NS160, CTEV, LC160
General & Plastic Surgery
55d