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