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FDA 510(k)

Qualis (linofilcon A) Soft (Hydrophilic) Daily Wear Contact Lens

K-Number: K213216 · 2022-01-18

Decision Date2022-01-18
Product CodeLPL
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

Qualis (linofilcon A) Soft (Hydrophilic) Daily Wear Contact Lens is a medical device manufactured by Unicon Optical Co., Ltd.. It received FDA 510(k) clearance on 2022-01-18 under approval number K213216. 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 Qualis (linofilcon A) Soft (Hydrophilic) Daily Wear Contact Lens?

Qualis (linofilcon A) Soft (Hydrophilic) Daily Wear Contact Lens is a medical device that received FDA 510(k) clearance on 2022-01-18. It is manufactured by Unicon Optical Co., Ltd.. The 510(k) number is K213216.

When was Qualis (linofilcon A) Soft (Hydrophilic) Daily Wear Contact Lens approved by the FDA?

Qualis (linofilcon A) Soft (Hydrophilic) Daily Wear Contact Lens received FDA 510(k) clearance on 2022-01-18, under approval number K213216.

What company makes Qualis (linofilcon A) Soft (Hydrophilic) Daily Wear Contact Lens?

Qualis (linofilcon A) Soft (Hydrophilic) Daily Wear Contact Lens is manufactured by Unicon Optical Co., Ltd..

What is the FDA product code for Qualis (linofilcon A) Soft (Hydrophilic) Daily Wear Contact Lens?

The FDA product code for Qualis (linofilcon A) Soft (Hydrophilic) Daily Wear Contact Lens is LPL.

Related Clinical Trials

Other Devices by Unicon Optical Co., Ltd.

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.