QUADROSTAR 532— 510(k) K060457

Substantially Equivalent

Asclepion Laser Technologies GmbH

FDA 510(k) clearance K060457 for QUADROSTAR 532, Substantially Equivalent on 2006-03-20. Applicant: Asclepion Laser Technologies GmbH.

Clearance details

Applicant: Asclepion Laser Technologies GmbH
Product code: Code GEX
Advisory panel: General, Plastic Surgery
Date received: 2006-02-22
Decision date: 2006-03-20
Decision: Substantially Equivalent
Clearance type: Special
Location: Jena, DE

Download summary PDF View on FDA.gov ↗

Adverse events under product code GEX

product code GEX

Death: 33
Injury: 3,045
Malfunction: 12,903
Other: 25
Total: 16,006

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.