Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3016577639

FEI Number

3016577639

Entity Name

ACOSTA MEDICAL GROUP INC.

City/State/Country

Houston, TX, US

Establishment Address

363 N Sam Houston Parkway , East, Suite 1100, Houston, TX 77090, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Acosta Medical Group Inc. (Owner Number: 10090887)

Owner / Operator Contact Address

363 N Sam Houston Parkway , East, Suite 1100, Houston, TX 77090, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Acosta Uro-Gard

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NNW	Bag, Urine Collection, Leg, For External Use, Non-Sterile	Gastroenterology, Urology	Class 1	876.5250	2024-05-28

Official Correspondent

Alfredo Acosta

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Acosta Medical Group 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 3016577639. Last updated year: 2026. Please use registration number 3016577639 when referencing this establishment in official correspondence.