Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1000220575

FEI Number

1000220575

Entity Name

SOPER BROTHERS & ASSOCIATES

City/State/Country

HOUSTON, TX, US

Establishment Address

3355 W Alabama St Ste 830, HOUSTON, TX 77098, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

SOPER BROTHERS & ASSOCIATES (Owner Number: 9076439)

Owner / Operator Contact Address

3355 West Alabama Suite 830, --, Houston, TX 77098, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

OPHTHALMIC CONFORMER Custom Artificial Eye Single Use NON-CUSTOM ARTIFICIAL EYE SCLERAL SHELL

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HQN	Conformer, Ophthalmic	Ophthalmic	Class 2	886.3130	2005-08-15
HQH	Eye, Artificial, Non-Custom	Ophthalmic	Class 1	886.3200	2005-08-15
HQT	Shell, Scleral	Ophthalmic	Class 2	886.3800	2005-08-15

Official Correspondent

MARCUS SOPER

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

SOPER BROTHERS & ASSOCIATES

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 1000220575. Last updated year: 2026. Please use registration number 1000220575 when referencing this establishment in official correspondence.