CYNOSURE 1064NM DIODE LASER— 510(k) K123971

Substantially Equivalent

Cynosure, Inc.

FDA 510(k) clearance K123971 for CYNOSURE 1064NM DIODE LASER, Substantially Equivalent on 2013-05-02. Applicant: Cynosure, Inc..

Clearance details

Applicant: Cynosure, Inc.
Product code: Code ILY
Advisory panel: Physical Medicine
Date received: 2012-12-26
Decision date: 2013-05-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wesford, MA, US

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Adverse events under product code ILY

product code ILY

Death: 3
Total: 3

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.