Clariti 1 day (somofilcon A) Soft (Hydrophilic) Daily Disposable Contact Lens with UV Blocker
K-Number: K181920 · 2018-12-11
Device Summary
Frequently Asked Questions
What is the Clariti 1 day (somofilcon A) Soft (Hydrophilic) Daily Disposable Contact Lens with UV Blocker?
Clariti 1 day (somofilcon A) Soft (Hydrophilic) Daily Disposable Contact Lens with UV Blocker is a medical device that received FDA 510(k) clearance on 2018-12-11. It is manufactured by CooperVision, Inc.. The 510(k) number is K181920.
When was Clariti 1 day (somofilcon A) Soft (Hydrophilic) Daily Disposable Contact Lens with UV Blocker approved by the FDA?
Clariti 1 day (somofilcon A) Soft (Hydrophilic) Daily Disposable Contact Lens with UV Blocker received FDA 510(k) clearance on 2018-12-11, under approval number K181920.
What company makes Clariti 1 day (somofilcon A) Soft (Hydrophilic) Daily Disposable Contact Lens with UV Blocker?
Clariti 1 day (somofilcon A) Soft (Hydrophilic) Daily Disposable Contact Lens with UV Blocker is manufactured by CooperVision, Inc..
What is the FDA product code for Clariti 1 day (somofilcon A) Soft (Hydrophilic) Daily Disposable Contact Lens with UV Blocker?
The FDA product code for Clariti 1 day (somofilcon A) Soft (Hydrophilic) Daily Disposable Contact Lens with UV Blocker is LPL.
Related Clinical Trials
Other Devices by CooperVision, Inc.
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.