EYEREVE (hioxifilcon D) Soft (hydrophilic) Contact Lens for Daily Wear
K-Number: K161124 · 2016-08-26
Device Summary
Frequently Asked Questions
What is the EYEREVE (hioxifilcon D) Soft (hydrophilic) Contact Lens for Daily Wear?
EYEREVE (hioxifilcon D) Soft (hydrophilic) Contact Lens for Daily Wear is a medical device that received FDA 510(k) clearance on 2016-08-26. It is manufactured by Vision Science Co., Ltd.. The 510(k) number is K161124.
When was EYEREVE (hioxifilcon D) Soft (hydrophilic) Contact Lens for Daily Wear approved by the FDA?
EYEREVE (hioxifilcon D) Soft (hydrophilic) Contact Lens for Daily Wear received FDA 510(k) clearance on 2016-08-26, under approval number K161124.
What company makes EYEREVE (hioxifilcon D) Soft (hydrophilic) Contact Lens for Daily Wear?
EYEREVE (hioxifilcon D) Soft (hydrophilic) Contact Lens for Daily Wear is manufactured by Vision Science Co., Ltd..
What is the FDA product code for EYEREVE (hioxifilcon D) Soft (hydrophilic) Contact Lens for Daily Wear?
The FDA product code for EYEREVE (hioxifilcon D) Soft (hydrophilic) Contact Lens for Daily Wear is LPL.
Related Clinical Trials
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.