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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 the device name listed in this FDA 510(k) record. The listed applicant is Unicon Optical Co., Ltd.. It received FDA 510(k) clearance on 2022-01-18 under 510(k) 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. The listed applicant is Unicon Optical Co., Ltd.. The 510(k) number is K213216.

When did Qualis (linofilcon A) Soft (Hydrophilic) Daily Wear Contact Lens receive FDA 510(k) clearance?

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

Who is the listed applicant for Qualis (linofilcon A) Soft (Hydrophilic) Daily Wear Contact Lens?

The FDA 510(k) record lists Unicon Optical Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

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

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Unicon Optical Co., Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: LPL)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.