Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by CYDEN LIMITED
FDA 510(k) Number
Submission Date
Device Name
Applicant
K200184
01/24/2020
SmoothSkin Pure
CyDen Limited
K190354
02/15/2019
BRAUN Silk.expert Pro 5
CyDen Limited
K190366
02/15/2019
BRAUN Silk Expert Pro 3
CyDen Limited
K230911
03/31/2023
Braun Skin i.expert
CyDen Limited
K211994
06/28/2021
Braun Silk.expert Mini
CyDen Limited
K192010
07/29/2019
SmoothSkin BARE+
CyDen Limited
K213692
11/23/2021
SmoothSkin Pure Mini
CyDen Limited
K122280
07/30/2012
IPULSE SMOOTHSKIN HAIR REMOVAL SYSTEM
CYDEN LIMITED
K130315
02/08/2013
IPULSE HAIR REMOVAL SYSTEM
CYDEN LIMITED
K071883
07/09/2007
IPULSE, QUADRA Q4 PLATINUM SERIES, MODEL(S) 1200+SERIES 2, 1300 SERIES 2, Q4 SERIES 2
CYDEN LIMITED
K083748
12/17/2008
IPULSE, MODEL: I150
CYDEN LIMITED
K040156
01/23/2004
IFL PROFESSIONAL SYSTEM, MODEL C100
CYDEN LIMITED
K050165
01/25/2005
MODIFICATION TO IFL PROFESSIONAL SYSTEM, MODEL C100
CYDEN LIMITED
K080406
02/14/2008
IPULSE, MODEL I400
CYDEN LIMITED
K170734
03/10/2017
Venus Silk.expert
Cyden Limited
K160968
04/06/2016
iPulse SmoothSkin Gold Hair Removal Device
CYDEN LIMITED
K162231
08/08/2016
iPulse SmoothSkin Gold Hair Removal Device, Venus Silk.expert
CYDEN LIMITED
K163552
12/19/2016
iPulse SmoothSkin BARE Hair Removal Device
CYDEN LIMITED
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact