TRI-BEAM PRO, TRI-BEAM (Nd:YAG Laser unit)— 510(k) K251464

Substantially Equivalent

Jeisys Medical Incorporated

FDA 510(k) clearance K251464 for TRI-BEAM PRO, TRI-BEAM (Nd:YAG Laser unit), Substantially Equivalent on 2025-10-03. Applicant: Jeisys Medical Incorporated.

Clearance details

Applicant: Jeisys Medical Incorporated
Product code: Code GEX
Advisory panel: General, Plastic Surgery
Date received: 2025-05-13
Decision date: 2025-10-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Seoul, KR

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.