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