Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3005572604

FEI Number

3005572604

Entity Name

The Allied Group, LLC

City/State/Country

Cumberland, RI, US

Establishment Address

30 Martin St, Cumberland, RI 02864, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

Allied Group LLC (Owner Number: 10060039)

Owner / Operator Contact Address

30 Martin Street, Suite 2C1, Cumberland, RI 02864, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Specimen Mailer Product

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KDW	Container, Specimen Mailer And Storage, Temperature Controlled, Sterile	Pathology	Class 1	864.3250	2019-03-22

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Allied Group LLC

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K913967	Doxtech, Inc.	DOX TAMPERPROOF SPECIMEN CONTAINER SYSTEM	1991-10-18

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005572604. Last updated year: 2026. Please use registration number 3005572604 when referencing this establishment in official correspondence.