Cyden Limited
Cyden Limited appears in FDA public data with 0 recalls, 21 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Nov 27, 2024.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 21
- Inspections
- 1
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K243362 | SmoothSkin Pure Switch (SSC1) | Nov 27, 2024 |
| K240587 | SmoothSkin Pure Unplugged (SSB3) | Mar 29, 2024 |
| K233782 | SmoothSkin Pure Adapt (SSG3) | Dec 20, 2023 |
| K230911 | Braun Skin i.expert | Apr 27, 2023 |
| K213692 | SmoothSkin Pure Mini | Jan 26, 2022 |
| K211994 | Braun Silk.expert Mini | Jul 28, 2021 |
| K200184 | SmoothSkin Pure | Feb 21, 2020 |
| K192010 | SmoothSkin BARE+ | Sep 24, 2019 |
| K190354 | BRAUN Silk.expert Pro 5 | Mar 18, 2019 |
| K190366 | BRAUN Silk Expert Pro 3 | Mar 18, 2019 |
| K170734 | Venus Silk.expert | May 8, 2017 |
| K163552 | iPulse SmoothSkin BARE Hair Removal Device | Mar 3, 2017 |
| K162231 | iPulse SmoothSkin Gold Hair Removal Device, Venus Silk.expert | Nov 16, 2016 |
| K160968 | iPulse SmoothSkin Gold Hair Removal Device | Apr 14, 2016 |
| K130315 | IPULSE HAIR REMOVAL SYSTEM | Jul 12, 2013 |
| K122280 | IPULSE SMOOTHSKIN HAIR REMOVAL SYSTEM | Oct 23, 2012 |
| K083748 | IPULSE, MODEL: I150 | Feb 2, 2009 |
| K080406 | IPULSE, MODEL I400 | Mar 10, 2008 |
| K071883 | IPULSE, QUADRA Q4 PLATINUM SERIES, MODEL(S) 1200+SERIES 2, 1300 SERIES 2, Q4 SERIES 2 | Jan 23, 2008 |
| K050165 | MODIFICATION TO IFL PROFESSIONAL SYSTEM, MODEL C100 | Apr 19, 2005 |