Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3044036787

FEI Number

3044036787

Entity Name

UTP Solutions

City/State/Country

Evart, MI, US

Establishment Address

5843 100th Ave, Evart, MI 49631, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Medi-Tec Plastics, LLC (Owner Number: 10095552)

Owner / Operator Contact Address

5843 100th Ave, Evart, MI 49631, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GCB	Needle, Catheter	General, Plastic Surgery	Class 1	878.4200	2026-03-28

Official Correspondent

Ryan Eggleston

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Medi-Tec Plastics, 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 3044036787. Last updated year: 2026. Please use registration number 3044036787 when referencing this establishment in official correspondence.