Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3041107043

FEI Number

3041107043

Entity Name

WILLOW TREE SOLUTIONS, LLC

City/State/Country

East Hartford, CT, US

Establishment Address

221 Park Ave, East Hartford, CT 06108, US

Establishment Type(s)

Repack or Relabel Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Willow Tree Solutions, LLC (Owner Number: 10094505)

Owner / Operator Contact Address

221 Park Ave, East Hartford, CT 06108, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Advance Dx

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NNK	Container, Specimen Mailer And Storage, Non-Sterile	Pathology	Class 1	864.3250	2025-12-04

Official Correspondent

Jeffrey Grote

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Willow Tree Solutions, 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 3041107043. Last updated year: 2026. Please use registration number 3041107043 when referencing this establishment in official correspondence.