Endophotonix, Inc. is one of 23683 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Endophotonix, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SOLAR LASER ABLATION SYSTEM, MODELS: LU-1083-25, LF-1083, PC-1000, IC-1083, LW-2000, LG-2001, LK-001, PM-1083, TF-1083
1
Total
1
Cleared
0
Denied
Endophotonix, Inc. has 1 FDA 510(k) cleared medical devices. Based in Inver Grove Heights, US.
Historical record: 1 cleared submissions from 2009 to 2009. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Endophotonix, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Endophotonix, Inc.
1 devices