Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3005065295

FEI Number

3005065295

Entity Name

DURABUILT MEDICAL CORP.

City/State/Country

TEXARKANA, AR, US

Establishment Address

1901 EAST 50TH ST., TEXARKANA, AR 71854, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

DURABUILT MEDICAL CORP. (Owner Number: 9071255)

Owner / Operator Contact Address

1901 EAST 50TH ST., --, Texarkana, AR 71854, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Durabuilt

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LGX	Table, Examination, Medical, Powered	General, Plastic Surgery	Class 1	878.4960	2005-03-11

Official Correspondent

Tony Asbille

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

DURABUILT MEDICAL CORP.

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 3005065295. Last updated year: 2026. Please use registration number 3005065295 when referencing this establishment in official correspondence.