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Cyden Limited

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
21
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K243362SmoothSkin Pure Switch (SSC1)November 27, 2024
K240587SmoothSkin Pure Unplugged (SSB3)March 29, 2024
K233782SmoothSkin Pure Adapt (SSG3)December 20, 2023
K230911Braun Skin i.expertApril 27, 2023
K213692SmoothSkin Pure MiniJanuary 26, 2022
K211994Braun Silk.expert MiniJuly 28, 2021
K200184SmoothSkin PureFebruary 21, 2020
K192010SmoothSkin BARE+September 24, 2019
K190354BRAUN Silk.expert Pro 5March 18, 2019
K190366BRAUN Silk Expert Pro 3March 18, 2019
K170734Venus Silk.expertMay 8, 2017
K163552iPulse SmoothSkin BARE Hair Removal DeviceMarch 3, 2017
K162231iPulse SmoothSkin Gold Hair Removal Device, Venus Silk.expertNovember 16, 2016
K160968iPulse SmoothSkin Gold Hair Removal DeviceApril 14, 2016
K130315IPULSE HAIR REMOVAL SYSTEMJuly 12, 2013
K122280IPULSE SMOOTHSKIN HAIR REMOVAL SYSTEMOctober 23, 2012
K083748IPULSE, MODEL: I150February 2, 2009
K080406IPULSE, MODEL I400March 10, 2008
K071883IPULSE, QUADRA Q4 PLATINUM SERIES, MODEL(S) 1200+SERIES 2, 1300 SERIES 2, Q4 SERIES 2January 23, 2008
K050165MODIFICATION TO IFL PROFESSIONAL SYSTEM, MODEL C100April 19, 2005