Viora , Ltd. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Viora , Ltd. has 11 FDA 510(k) cleared general & plastic surgery devices. Based in Jersey City, US.
Historical record: 11 cleared submissions from 2009 to 2020.
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.
FDA 510(k) cleared devices by Viora , Ltd.
11 devices
Cleared
Dec 09, 2020
V30 system, V20 system, V10 system, V-VR Hand piece
General & Plastic Surgery
121d
Cleared
Jul 15, 2020
V30 System, V20 System, V10 System, V-FR Handpiece
General & Plastic Surgery
85d
Cleared
May 21, 2020
V30 system, V20 system, V10 system, V-FC Handpiece
General & Plastic Surgery
85d
Cleared
Nov 18, 2016
V30 system, V-Form Handpiece BC Medium applicator
General & Plastic Surgery
87d
Cleared
Feb 19, 2016
V20 system
General & Plastic Surgery
158d
Cleared
May 01, 2015
V10 system
General & Plastic Surgery
112d
Cleared
Nov 14, 2014
V20 SYSTEM
General & Plastic Surgery
105d
Cleared
Oct 21, 2014
VIORA V-TOUCH
General & Plastic Surgery
99d
Cleared
Apr 09, 2014
VIORA V-TOTAL
General & Plastic Surgery
112d
Cleared
Jul 01, 2009
REACTION SYSTEM
General & Plastic Surgery
152d
Cleared
Jun 10, 2009
TRIOS SYSTEM
General & Plastic Surgery
113d