Litecure, LLC - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Litecure, LLC has 7 FDA 510(k) cleared medical devices. Based in Newark, US.
Historical record: 7 cleared submissions from 2007 to 2018. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Litecure, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Litecure, LLC
7 devices
Cleared
Feb 22, 2018
LightForce LTS Model 1000, 1500, 2500, and 4000
General & Plastic Surgery
146d
Cleared
Mar 29, 2013
LITECURE THERAPY SYSTEM MODEL LTS-1500
General & Plastic Surgery
183d
Cleared
Dec 03, 2012
BWF-5 MEDICAL LASER SERIES
General & Plastic Surgery
66d
Cleared
Jun 12, 2012
LITECURE THERAPY COMPACT
Physical Medicine
25d
Cleared
Jan 25, 2011
LITECURE THERAPY SYSTEM
Physical Medicine
56d
Cleared
May 12, 2010
BWF-5 MEDICAL LASER SERIES
General & Plastic Surgery
223d
Cleared
Feb 28, 2007
LC THERAPY, MODEL LCT-1000
Physical Medicine
16d