Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3033985519

FEI Number

3033985519

Entity Name

DISTRIBUTED MEDICAL DEVICE MANUFACTURING LLC.

City/State/Country

Tucson, AZ, US

Establishment Address

657 W Saint Marys Rd, Tucson, AZ 85701, US

Establishment Type(s)

Repack or Relabel Medical Device,Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device

Owner / Operator

Distributed Medical Device Manufacturing LLC. (Owner Number: 10092150)

Owner / Operator Contact Address

657 W Saint Marys Rd, Tucson, AZ 85701, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

DMDM TQ1

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GAX	Tourniquet, Nonpneumatic	General, Plastic Surgery	Class 1	878.5900	2024-12-09

Official Correspondent

Alex Barton

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Distributed Medical Device Manufacturing LLC.

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 3033985519. Last updated year: 2026. Please use registration number 3033985519 when referencing this establishment in official correspondence.