Laser Fiber (PT-OF-A-S); Laser Fiber (PT-OF-B-S); Laser Fiber (PT-OF-C-S); Laser Fiber (PT-OF-D-S); Laser Fiber (PT-OF-E-S); Laser Fiber (PT-OF-F-S)— 510(k) K253007

Substantially Equivalent

Guangzhou Potent Medical Equipment Joint-Stock Co., Ltd.

FDA 510(k) clearance K253007 for Laser Fiber (PT-OF-A-S); Laser Fiber (PT-OF-B-S); Laser Fiber (PT-OF-C-S); Laser Fiber (PT-OF-D-S); Laser Fiber (PT-OF-E-S); Laser Fiber (PT-OF-F-S), Substantially Equivalent on 2025-11-20. Applicant: Guangzhou Potent Medical Equipment Joint-Stock Co., Ltd..

Clearance details

Applicant: Guangzhou Potent Medical Equipment Joint-Stock Co., Ltd.
Product code: Code GEX
Advisory panel: General, Plastic Surgery
Date received: 2025-09-19
Decision date: 2025-11-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Guangzhou, CN

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.