Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3042953262

FEI Number

3042953262

Entity Name

DALLAS EYE PROSTHETICS

City/State/Country

Dallas, TX, US

Establishment Address

4600 Greenville Ave Ste 240, Dallas, TX 75206, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Dallas Eye Prosthetics (Owner Number: 10094700)

Owner / Operator Contact Address

4600 Greenville Ave., Suite 240, Dallas, TX 75206, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

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
HQT	Shell, Scleral	Ophthalmic	Class 2	886.3800	2025-12-17
HQN	Conformer, Ophthalmic	Ophthalmic	Class 2	886.3130	2025-12-17
NCK	Button, Iris, Eye, Artificial	Ophthalmic	Class 1	886.3200	2025-12-17

Official Correspondent

John Trawnik

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Dallas Eye Prosthetics

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

View Entity Profile →

Similar Registrations

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3042228518	AKRITI OPHTHALMIC PRIVATE LIMITED	Hyderabad Telangana, IN
2183958	MIDWEST EYE LABORATORIES, INC.	ROCHESTER, MN, US
3007096749	LIGHTS' PROSTHETIC EYES, INC.	Peoria, IL, US
3003951061	M/S TARUN ENTERPRISES	Prayagraj, Uttar Pradesh, IN
2183831	MIDWEST EYE LABORATORIES WOODBURY LLC	Saint Paul, MN, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3042953262. Last updated year: 2026. Please use registration number 3042953262 when referencing this establishment in official correspondence.