SILKPRO Titanium Diode Laser System SILKPRO-S20S-TWC— 510(k) K222862

Substantially Equivalent

Lotuxs Medtech (Suzhou) Co., Ltd.

FDA 510(k) clearance K222862 for SILKPRO Titanium Diode Laser System SILKPRO-S20S-TWC, Substantially Equivalent on 2023-07-30. Applicant: Lotuxs Medtech (Suzhou) Co., Ltd..

Clearance details

Applicant: Lotuxs Medtech (Suzhou) Co., Ltd.
Product code: Code GEX
Advisory panel: General, Plastic Surgery
Date received: 2022-09-22
Decision date: 2023-07-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Suzhou Industrial Park, Suzhou, 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.