ClearanceBrief
Company ยท IL

Viora , Ltd.

FDA 510(k) clearances and medical device recalls filed under this name, 2009 to 2020. Name variants (Inc, Corp, punctuation) are merged.

11510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
GEXPowered Laser Surgical Instrument4
PBXMassager, Vacuum, Radio Frequency Induced Heat4
GEIElectrosurgical, Cutting & Coagulation & Accessories1
NUVMassager, Vacuum, Light Induced Heating1
ONFPowered Light Based Non-Laser Surgical Instrument With Thermal Effect1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Dec 9, 2020K202247V30 system, V20 system, V10 system, V-VR Hand piece
Viora , Ltd., IL
PBX
Jul 15, 2020K201064V30 System, V20 System, V10 System, V-FR Handpiece
Viora , Ltd., IL
PBX
May 21, 2020K200468V30 system, V20 system, V10 system, V-FC Handpiece
Viora , Ltd., IL
PBX
Nov 18, 2016K162363V30 system, V-Form Handpiece BC Medium applicator
Viora , Ltd., IL
GEX
Feb 19, 2016K152611V20 system
Viora , Ltd., IL
GEX
May 1, 2015K150035V10 system
Viora , Ltd., IL
PBX
Nov 14, 2014K142093V20 SYSTEM
Viora , Ltd., IL
GEX
Oct 21, 2014K141904VIORA V-TOUCH
Viora , Ltd., IL
GEI
Apr 9, 2014K133837VIORA V-TOTAL
Viora , Ltd., IL
GEX
Jul 1, 2009K090221REACTION SYSTEM
Viora , Ltd.
NUV
Jun 10, 2009K090399TRIOS SYSTEM
Viora , Ltd.
ONF

Latest recalls

DateFirm and productCodeLinked 510(k)
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