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Cynosure

Medical device maker in United States, part of Hologic. FDA records under 5 spellings of its name, each linked to the record.

  • 510(k) clearances: 108
  • Device recalls: 1

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
Jun 17, 2026PICOSURE WORKSTATIONK261570 · GEX510(k) clearances
Mar 8, 2024Elite iQ PRO (M122K1)K240396 · GEX510(k) clearances
Jul 6, 2023MyEllevateK230510 · GAT510(k) clearances
Nov 23, 2022TempSure SystemK223292 · GEI510(k) clearances
Mar 18, 2022TempSure SystemK212891 · GEI510(k) clearances
Mar 30, 2021PicoSure WorkstationK210226 · GEX510(k) clearances
Mar 25, 2020TempSure SystemK200241 · PBX510(k) clearances
Mar 9, 2020Elite iQK193426 · GEX510(k) clearances

Canada and Imports

Matched by company name
Active Health Canada device licences
29, as of Nov 10, 2026
FDA import refusals since 2024
2 shipment lines, through Oct 23, 2026

Names and Identifiers

Appears as
Cynosure, Inc.Cynosure, LLCCynosure, Inc. Dba EllmanCynosure

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.