Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3016440358

FEI Number

3016440358

Entity Name

DRY EYE INNOVATIONS, LLC

City/State/Country

Franklin, TN, US

Establishment Address

5051 Kathryn Ave, Franklin, TN 37064, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Dry Eye Innovations, LLC (Owner Number: 10062370)

Owner / Operator Contact Address

1441 New Highway 96 W, Suite 2-407, Franklin, TN 37064, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K201069

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MRC	Products, Contact Lens Care, Rigid Gas Permeable	Ophthalmic	Class 2	886.5918	2020-11-17

Official Correspondent

Donald Sanders

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Dry Eye Innovations, LLC

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0030-2022	Contamac Solutions, Inc.	2	Nutrifill Scleral, Hybrid, and Gas Permeable (GP) Lens Insertion Solution, Physiologic Formula, Preservative Free, 35 Single-use 10ml ampoules (360ml), UDI:00850012123002

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3016440358. Last updated year: 2026. Please use registration number 3016440358 when referencing this establishment in official correspondence.