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FDA 510(k)

Lucens 41 (senofilcon C) Silicone Hydrogel Soft (Hydrophilic) Contact Lens

K-Number: K242391 · 2024-10-08

Decision Date2024-10-08
Product CodeLPL
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

Lucens 41 (senofilcon C) Silicone Hydrogel Soft (Hydrophilic) Contact Lens is a medical device manufactured by Lucens Technology Co., Ltd.. It received FDA 510(k) clearance on 2024-10-08 under approval number K242391. The device is classified under product code LPL. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Lucens 41 (senofilcon C) Silicone Hydrogel Soft (Hydrophilic) Contact Lens?

Lucens 41 (senofilcon C) Silicone Hydrogel Soft (Hydrophilic) Contact Lens is a medical device that received FDA 510(k) clearance on 2024-10-08. It is manufactured by Lucens Technology Co., Ltd.. The 510(k) number is K242391.

When was Lucens 41 (senofilcon C) Silicone Hydrogel Soft (Hydrophilic) Contact Lens approved by the FDA?

Lucens 41 (senofilcon C) Silicone Hydrogel Soft (Hydrophilic) Contact Lens received FDA 510(k) clearance on 2024-10-08, under approval number K242391.

What company makes Lucens 41 (senofilcon C) Silicone Hydrogel Soft (Hydrophilic) Contact Lens?

Lucens 41 (senofilcon C) Silicone Hydrogel Soft (Hydrophilic) Contact Lens is manufactured by Lucens Technology Co., Ltd..

What is the FDA product code for Lucens 41 (senofilcon C) Silicone Hydrogel Soft (Hydrophilic) Contact Lens?

The FDA product code for Lucens 41 (senofilcon C) Silicone Hydrogel Soft (Hydrophilic) Contact Lens is LPL.

Related Clinical Trials

Related Devices (Code: LPL)

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.