Cyden Limited
Cyden Limited holds FDA 510(k) medical device clearances, first cleared 2004, most recent 2026.
Name variants for Cyden Limited
as filed with FDA- Cyden Limited
- CyDen Limited
Top product codes for Cyden Limited
Recent clearances by Cyden Limited
- K261975 — Braun Aura 7 (6041)
- K261977 — Braun Aura 9 (6042)
- K243362 — SmoothSkin Pure Switch (SSC1)
- K240587 — SmoothSkin Pure Unplugged (SSB3)
- K233782 — SmoothSkin Pure Adapt (SSG3)
- K230911 — Braun Skin i.expert
- K213692 — SmoothSkin Pure Mini
- K211994 — Braun Silk.expert Mini
- K200184 — SmoothSkin Pure
- K192010 — SmoothSkin BARE+
- K190354 — BRAUN Silk.expert Pro 5
- K190366 — BRAUN Silk Expert Pro 3
- K170734 — Venus Silk.expert
- K163552 — iPulse SmoothSkin BARE Hair Removal Device
- K162231 — iPulse SmoothSkin Gold Hair Removal Device, Venus Silk.expert
- K160968 — iPulse SmoothSkin Gold Hair Removal Device
- K130315 — IPULSE HAIR REMOVAL SYSTEM
- K122280 — IPULSE SMOOTHSKIN HAIR REMOVAL SYSTEM
- K083748 — IPULSE, MODEL: I150
- K080406 — IPULSE, MODEL I400
- K071883 — IPULSE, QUADRA Q4 PLATINUM SERIES, MODEL(S) 1200+SERIES 2, 1300 SERIES 2, Q4 SERIES 2
- K050165 — MODIFICATION TO IFL PROFESSIONAL SYSTEM, MODEL C100
- K040156 — IFL PROFESSIONAL SYSTEM, MODEL C100
Data sourced from openFDA. This site is unofficial and independent of the FDA.