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CyDen

Medical device maker. FDA records under 2 spellings of its name, each linked to the record.

  • 510(k) clearances: 23

Records by Year

Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date

Latest Records

Newest first across sources; each opens the record
DateRecordSource
Sep 30, 2026Braun Aura 7 (6041)K261975 · OHT510(k) clearances
Sep 25, 2026Braun Aura 9 (6042)K261977 · OHT510(k) clearances
Nov 27, 2024SmoothSkin Pure Switch (SSC1)K243362 · OHT510(k) clearances
Mar 29, 2024SmoothSkin Pure Unplugged (SSB3)K240587 · OHT510(k) clearances
Dec 20, 2023SmoothSkin Pure Adapt (SSG3)K233782 · OHT510(k) clearances
Apr 27, 2023Braun Skin i.expertK230911 · OHT510(k) clearances
Jan 26, 2022SmoothSkin Pure MiniK213692 · OHT510(k) clearances
Jul 28, 2021Braun Silk.expert MiniK211994 · OHT510(k) clearances

Canada and Imports

Matched by company name
Active Health Canada device licences
5, as of Nov 10, 2026

Names and Identifiers

Appears as
Cyden LimitedCyDen Limited

Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built

Logos are each company's own site icon, matched by name through Wikidata.Company names and logos identify the companies in public FDA and registry records and do not imply endorsement.