Who else makes this device?

Name: VibrantVue
Brand: VibrantVue

Ophthalmic › TherapeuticProducts, Contact Lens Care, Rigid Gas Permeable

VibrantVue

Sterile, preservative-free, unbuffered saline solution in a single dose 5 ml vial.

Registry build 21.09.26

1manufacturer

2catalogue numbers in this listing

1510(k) clearance

Who Else Makes It

Registered in Zhejiang.

Chinese manufacturers registered for FDA product code MRC
Manufacturer	City	Province	Registered as	Device types
AMO (Hangzhou) Co., Ltd.	Hangzhou	Zhejiang	Manufacturer	2

Record

Regulatory record for VibrantVue
Listed by	DRY EYE Innovations, LLC, United States
FDA product code	MRC
Device type	Products, Contact Lens Care, Rigid Gas Permeable
Device class	Class 2
Regulation	21 CFR 886.5918
Establishment	Specification developer, Repacker / relabeller, Manufacturer
Record published	2025-12-01
Record revised	2026-03-16 (version 2)

Specifications

Specifications
MRI safety	Labeling does not contain MRI Safety Information
Supplied sterile	Yes
Single use	Yes
Over the counter	Yes
Storage	Storage environment temperature from 32 °F; Storage environment temperature from 0 °C

Catalogue Numbers

Catalogue numbers for VibrantVue
Catalogue number	Size	Status
VibrantVue Saline Samples		In distribution
VibrantVue Saline		In distribution

Same Product Code

Other products under the same FDA product code
Product	Sold by	Catalogue numbers
Bausch + Lomb	Bausch & Lomb Incorporated	15
Menicon Unique pH Multi-Purpose Solution	Menicon America, Inc.	3
Equate	Wal Mart Stores, Inc	3
Menicon Progent Protein Remover	Menicon America, Inc.	2
Nutrifill	Contamac Solutions, Inc.	2
Tangible Clean Sample Bottle	Tangible Science Inc	2
Tangible Clean	Tangible Science Inc	2
cleadew GP hydra one	Ophtecs Corporation	2
PuriLens Plus Preservative Free Saline	Lifestyle Co Inc, THE	2
Meijer	Meijer, Inc.	2
up & up rigid gas permeable contact lens conditioning solution	Target Health, Inc.	1
Tangible Fill	DRY EYE Innovations, LLC	1

Showing 12 of 18. All products under Products, Contact Lens Care, Rigid Gas Permeable

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance	Decision date
K201069	2020-07-31

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.