Litecure, LLC - FDA 510(k) Cleared Devices
Recent clearances: LightForce LTS Model 1000, 1500, 2500, and 4000
7
Total
7
Cleared
0
Denied
FDA 510(k) Regulatory Record - Litecure, LLC General & Plastic Surgery ✕
4 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
May 12, 2010
BWF-5 MEDICAL LASER SERIES
General & Plastic Surgery
223d