FDA.reportPublic FDA data

VIORA LTD.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30056957243005695724VIORA LTD.1N2027-01-01Sagi 2000 Industrial Park Migdal HaEmek Northern IL 1812003

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
249871222125966K202247V30 system, V20 system, V10 system, V-VR Hand piecePBX2020-12-09
249871808454184K201064V30 System, V20 System, V10 System, V-FR HandpiecePBX2020-07-15
249872043863328K200468V30 system, V20 system, V10 system, V-FC HandpiecePBX2020-05-21
249871793924419K162363V30 system, V-Form Handpiece BC Medium applicatorGEX2016-11-18
249871107385944K152611V20 systemGEX2016-02-19
249871565517605K150035V10 systemPBX2015-05-01
249871895547382K142093V20 SYSTEMGEX2014-11-14
249871622078585K141904VIORA V-TOUCHGEI2014-10-21
249871814066679K133837VIORA V-TOTALGEX2014-04-09
249871423496195K090399TRIOS SYSTEMONF2009-06-10
249871845370149K090221REACTION SYSTEMNUV2009-07-01
249871223710791K082138AIRGENT, MODEL AG7000010KZE2009-01-23
249871072017477
249871717571216

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
GEX82016-11-18
PBX52020-12-09
NUV22009-07-01
ONF22009-06-10
GEI12014-10-21
KZE12009-01-23

PMN#