BEAMAX/ FORMAX PULSED LIGHT DEVICE FAMILY— 510(k) K082876

Substantially Equivalent

Sharplight Technologies, Ltd.

FDA 510(k) clearance K082876 for BEAMAX/ FORMAX PULSED LIGHT DEVICE FAMILY, Substantially Equivalent on 2008-11-10. Applicant: Sharplight Technologies, Ltd..

Clearance details

Applicant: Sharplight Technologies, Ltd.
Product code: Code GEX
Advisory panel: General, Plastic Surgery
Date received: 2008-09-29
Decision date: 2008-11-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Zichron Yaacov, IL

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.