Lightlab Imaging, Inc. is one of 22265 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Lightlab Imaging, Inc. - FDA 510(k) Cleared Devices
Recent clearances: OPTIS Metallic Stent Optimization E.4 SW, OPTIS Mobile System, OPTIS Integrated System Mobile Workstation
10
Total
10
Cleared
0
Denied
Lightlab Imaging, Inc. has 10 FDA 510(k) cleared general & plastic surgery devices. Based in Rockville, US.
Historical record: 10 cleared submissions from 2010 to 2016.
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.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Lightlab Imaging, Inc.
10 devices
Cleared
Jun 29, 2016
OPTIS Metallic Stent Optimization E.4 SW
General & Plastic Surgery
91d
Cleared
Oct 29, 2015
OPTIS Mobile System
General & Plastic Surgery
91d
Cleared
Aug 05, 2015
OPTIS Integrated System Mobile Workstation
General & Plastic Surgery
83d
Cleared
Jul 15, 2015
ILUMIEN OPTIS
General & Plastic Surgery
105d
Cleared
May 05, 2015
ILUMIEN, Drageonfly OPTIS Imaging Catheter
General & Plastic Surgery
92d
Cleared
Sep 19, 2014
ILUMIEN OPTIS, DRAGONFLY OPTIS IMAGING CATHETER
Cardiovascular
109d
Cleared
Aug 18, 2014
OPTIS INTEGRATED SYSTEM, DRAGONFLY OPTIS IMAGING CATHETER
Cardiovascular
48d
Cleared
Jan 30, 2013
ILUMIEN OPTIS
General & Plastic Surgery
90d
Cleared
Aug 10, 2011
C7 XR IMAGING SYSTEM
General & Plastic Surgery
103d
Cleared
CT
Apr 30, 2010
C7 XR IMAGING SYSTEM WITH C7 DRAGONFLY IMAGING CATHETER AND DISPOSABLE...
General & Plastic Surgery
135d