Beacon Promotions, Inc.

FDA Device Registration & Listing · Eagan, MN, US · Registration 3004305946

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3004305946
FEI Number
3004305946
Entity Name
Beacon Promotions, Inc.
City/State/Country
Eagan, MN, US
Establishment Address
980 Aldrin Dr, Eagan, MN 55121, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Beacon Promotions Inc DBA MIXIE (Owner Number: 10087047)
Owner / Operator Contact Address
980 Aldrin Dr, Eagan, MN 55121, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

DC03DF RFM RFMSM REP PC25PB PC24PB PC38CS PC31BB PC30BB

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JET Pick, Massaging Dental Class 1 872.6650 2024-06-04
IME Pack, Hot Or Cold, Reusable Physical Medicine Class 1 890.5700 2023-03-17
NXB Dispenser, Solid Medication Physical Medicine Class 1 890.5050 2024-05-10
KXF Applicator, Absorbent Tipped, Non-Sterile General Hospital Class 1 880.6025 2025-11-18
KGX Tape And Bandage, Adhesive General Hospital Class 1 880.5240 2024-11-15

Official Correspondent

John McMahon

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Beacon Promotions Inc DBA MIXIE
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
K821629 Moyco Industries, Inc. FIXIDENT 1982-06-14
K944481 Garan Scientific, Inc. THE HEART PROTECTOR 1995-04-10
K843874 Beiersdorf, Inc. LEUKOPOR SURGICAL TAPE 1985-02-21
K915446 Sun Glitz Corp. STRETCH WRAP 1992-05-06
K833120 Acme United Corp. ONE TIME COMPOUND BENZOIN TINCTURE- 1983-12-29

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004305946. Last updated year: 2026. Please use registration number 3004305946 when referencing this establishment in official correspondence.
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