Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3016734024

FEI Number

3016734024

Entity Name

UNIVERSALPROMO INC.

City/State/Country

Maple Grove, MN, US

Establishment Address

11229 91st Ave. N, Maple Grove, MN 55369, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

UniversalPromo Inc. (Owner Number: 10070596)

Owner / Operator Contact Address

11229 91st Ave. N, Maple Grove, MN 55369, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

UniversalPromo, Inc. UniversalPromo, Inc. UniversalPromo, Inc. UniversalPromo, Inc.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KYZ	Syringe, Irrigating (Non Dental)	General Hospital	Class 1	880.6960	2020-04-28
KCM	Dropper, Ent	Ear, Nose, Throat	Class 1	874.5220	2020-04-28
NXB	Dispenser, Solid Medication	Physical Medicine	Class 1	890.5050	2020-04-17
KYW	Container, Liquid Medication, Graduated	General Hospital	Class 1	880.6430	2020-04-28

Official Correspondent

Peter Will

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

UniversalPromo Inc.

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
K944481	Garan Scientific, Inc.	THE HEART PROTECTOR	1995-04-10

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2084346	MARINA MEDICAL INSTRUMENTS, INC.	Davie, FL, US
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3016734024. Last updated year: 2026. Please use registration number 3016734024 when referencing this establishment in official correspondence.