Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3007207818

FEI Number

3007207818

Entity Name

OPHTHALMIC SOLUTION INC.

City/State/Country

Knoxville, TN, US

Establishment Address

820 Corridor Park Blvd, Knoxville, TN 37932, US

Establishment Type(s)

Manufacture Device in the United States for Export Only

Owner / Operator

Ophthalmic Solution Inc. (Owner Number: 10026556)

Owner / Operator Contact Address

Ophthalmic Solution Inc, 820 Corridor Park Blvd, Knoxville, TN 37932, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

intraocular lens delivery system Mirado Vistaso

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MSS	Folders And Injectors, Intraocular Lens (Iol)	Ophthalmic	Class 1	886.4300	2012-12-07
NAA	Lens, Intraocular, Accommodative	Ophthalmic	Class 3	886.3600	2019-04-10

Official Correspondent

Neil Chaudhary

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Ophthalmic Solution Inc.

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

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007207818. Last updated year: 2026. Please use registration number 3007207818 when referencing this establishment in official correspondence.