Qualis (linofilcon A) Soft (Hydrophilic) Daily Wear Contact Lens
K-Number: K213216 · 2022-01-18
Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.