Venus Concept , Ltd. is one of 227 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Venus Concept , Ltd. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Venus Concept , Ltd. has 9 FDA 510(k) cleared medical devices. Based in Binyamina, IL.
Historical record: 9 cleared submissions from 2010 to 2017. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Venus Concept , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Venus Concept , Ltd.
9 devices
Cleared
Jan 11, 2017
Venus Velocity Diode Laser System
General & Plastic Surgery
103d
Cleared
Mar 21, 2016
Venus Versa System
General & Plastic Surgery
88d
Cleared
Jan 20, 2016
Venus Versa System
General & Plastic Surgery
117d
Cleared
Aug 04, 2015
Venus Legacy CX
General & Plastic Surgery
232d
Cleared
May 12, 2015
Venus Viva SR Device
General & Plastic Surgery
109d
Cleared
Jun 25, 2014
VENUS SWAN(MP)2
General & Plastic Surgery
106d
Cleared
Mar 02, 2012
VENUS FREEZE (MP)2 SYSTEM
General & Plastic Surgery
261d
Cleared
Oct 07, 2011
VENUS SWAN SYSTEM
General & Plastic Surgery
108d
Cleared
Nov 29, 2010
VENUS FREEZE SYSTEM
General & Plastic Surgery
272d