FDA 510(k) Applications Submitted by VIORA LTD.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K090221 |
01/30/2009 |
REACTION SYSTEM |
VIORA LTD. |
| K090399 |
02/17/2009 |
TRIOS SYSTEM |
VIORA LTD. |
| K150035 |
01/09/2015 |
V10 system |
VIORA LTD. |
| K142093 |
08/01/2014 |
V20 SYSTEM |
VIORA LTD. |
| K152611 |
09/14/2015 |
V20 system |
VIORA LTD. |
| K202247 |
08/10/2020 |
V30 system, V20 system, V10 system, V-VR Hand piece |
Viora Ltd. |
| K201064 |
04/21/2020 |
V30 System, V20 System, V10 System, V-FR Handpiece |
Viora Ltd. |
| K200468 |
02/26/2020 |
V30 system, V20 system, V10 system, V-FC Handpiece |
Viora Ltd. |
| K162363 |
08/23/2016 |
V30 system, V-Form Handpiece BC Medium applicator |
Viora Ltd. |
| K141904 |
07/14/2014 |
VIORA V-TOUCH |
VIORA LTD. |
| K133837 |
12/18/2013 |
VIORA V-TOTAL |
VIORA LTD. |
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