New Star Lasers, Inc. is one of 5830 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
Recent clearances: NS3000 Holmium Laser System, NS 2500 HOLMIUM LASER SYSTEM, COOLTOUCH
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.
510(k) submissions have been managed by Buckman Company, Inc. as regulatory consultant.
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