Lucens 41 (senofilcon C) Silicone Hydrogel Soft (Hydrophilic) Contact Lens— 510(k) K242391

Substantially Equivalent

Lucens Technology Co., Ltd.

FDA 510(k) clearance K242391 for Lucens 41 (senofilcon C) Silicone Hydrogel Soft (Hydrophilic) Contact Lens, Substantially Equivalent on 2024-10-08. Applicant: Lucens Technology Co., Ltd..

Clearance details

Applicant: Lucens Technology Co., Ltd.
Product code: Code LPL
Advisory panel: Ophthalmic
Date received: 2024-08-12
Decision date: 2024-10-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Zhubei City, TW

Download summary PDF View on FDA.gov ↗

Adverse events under product code LPL

product code LPL

Injury: 988
Other: 4
Total: 992

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.