Curae'Lase, Inc. is one of 5140 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Curae'Lase, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Curae'Lase, Inc. has 2 FDA 510(k) cleared medical devices. Based in Houston, US.
Historical record: 2 cleared submissions from 2005 to 2014. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Curae'Lase, Inc. Filter by specialty or product code using the sidebar.
Curae'Lase, Inc. — FDA 510(k) Products and Clearance History
2 devices
Cleared
Jan 10, 2014
CL10009 IR LASER
Physical Medicine
351d
Cleared
Dec 09, 2005
CURAE'LASE CL1000 IR LASER SYSTEM
Physical Medicine
23d