FDA.reportPublic FDA data

VENUS CONCEPT LTD.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30089153163008915316VENUS CONCEPT LTD.1N2026-01-01Hamelacha 1 St. Yokneam Illit Northern IL 2069812

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
1283401664626014K252845Venus Nova (FP-2001)GEI2025-11-06
1283402001280245K220592Venus BlissMAXPBX2022-04-27
1283401824001764K201164Venus Viva MD DeviceGEI2020-06-26
1283401050027677K200786Venus EpileveGEX2020-06-09
1283401332904666K191528Venus Legacy Pro DeviceGEI2019-09-06
1283401099292322K191065Venus VivaTMGEI2020-04-01
1283401474406270K190743Venus BlissPBX2019-06-25
1283402067742539K182094Family of Venus RF Systems - HealPBX2019-02-01
1283401782501873K162765Venus Velocity Diode Laser SystemGEX2017-01-11
1283401775155862K153717Venus Versa SystemONF2016-03-21
1283401823138522K152790Venus Versa SystemONF2016-01-20
1283401609637819K150161Venus Viva SR DeviceGEI2015-05-12
1283401168692046K143554Venus Legacy CXPBX2015-08-04
1283401948291327K142910Legacy BXGEI2014-12-19
1283401835559845K111670VENUS FREEZE (MP)2 SYSTEMGEI2012-03-02

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
GEI72025-11-06
PBX42022-04-27
GEX22020-06-09
ONF22016-03-21

PMN#