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FDA 510(k)

HPM38 (polymacon) Daily Wear Soft (hydrophilic) Contact Lens (HPM38)

K-Number: K241884 · 2025-03-20

Decision Date2025-03-20
Product CodeLPL
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

HPM38 (polymacon) Daily Wear Soft (hydrophilic) Contact Lens (HPM38) is a medical device manufactured by Hunan Haipuming Technology Co., Ltd.. It received FDA 510(k) clearance on 2025-03-20 under approval number K241884. 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 HPM38 (polymacon) Daily Wear Soft (hydrophilic) Contact Lens (HPM38)?

HPM38 (polymacon) Daily Wear Soft (hydrophilic) Contact Lens (HPM38) is a medical device that received FDA 510(k) clearance on 2025-03-20. It is manufactured by Hunan Haipuming Technology Co., Ltd.. The 510(k) number is K241884.

When was HPM38 (polymacon) Daily Wear Soft (hydrophilic) Contact Lens (HPM38) approved by the FDA?

HPM38 (polymacon) Daily Wear Soft (hydrophilic) Contact Lens (HPM38) received FDA 510(k) clearance on 2025-03-20, under approval number K241884.

What company makes HPM38 (polymacon) Daily Wear Soft (hydrophilic) Contact Lens (HPM38)?

HPM38 (polymacon) Daily Wear Soft (hydrophilic) Contact Lens (HPM38) is manufactured by Hunan Haipuming Technology Co., Ltd..

What is the FDA product code for HPM38 (polymacon) Daily Wear Soft (hydrophilic) Contact Lens (HPM38)?

The FDA product code for HPM38 (polymacon) Daily Wear Soft (hydrophilic) Contact Lens (HPM38) 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.