Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3031783617

FEI Number

3031783617

Entity Name

MCDOUGALL MEDTECH, LLC

City/State/Country

Dania Beach, FL, US

Establishment Address

1221 Stirling Rd Ste 109, Dania Beach, FL 33004, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

McDougall MedTech (Owner Number: 10091257)

Owner / Operator Contact Address

9871 SW 2nd St, Plantation, FL 33324, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Quicktube Chest Tube Device

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GBX	Catheter, Irrigation	General, Plastic Surgery	Class 1	878.4200	2025-06-12

Official Correspondent

Veronica McDougall

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

McDougall MedTech

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 3031783617. Last updated year: 2026. Please use registration number 3031783617 when referencing this establishment in official correspondence.