LUMENIS ULTRAPULSE ENCORE CARBON DIOXIDE SURGICAL LASERS AND DELIVERY DEVICE ACCESSORIES— 510(k) K022060

Substantially Equivalent

Lumenis, Inc.

FDA 510(k) clearance K022060 for LUMENIS ULTRAPULSE ENCORE CARBON DIOXIDE SURGICAL LASERS AND DELIVERY DEVICE ACCESSORIES, Substantially Equivalent on 2002-10-30. Applicant: Lumenis, Inc..

Clearance details

Applicant: Lumenis, Inc.
Product code: Code GEX
Advisory panel: General, Plastic Surgery
Date received: 2002-06-25
Decision date: 2002-10-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Santa Clara, CA, US

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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.