3M COMPANY

FDA Device Registration & Listing · BROOKINGS, SD, US · Registration 1717046

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
1717046
FEI Number
1717046
Entity Name
3M COMPANY
City/State/Country
BROOKINGS, SD, US
Establishment Address
601 22nd Ave S, BROOKINGS, SD 57006, US
Establishment Type(s)
Repack or Relabel Medical Device,Manufacture Medical Device
Owner / Operator
3M COMPANY (Owner Number: 2110898)
Owner / Operator Contact Address
2510 Conway Avenue, Saint Paul, MN 55144, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

BANDAGE, ELASTIC 3M Pack, hot or cold, reusable 3M STOMASEAL ADHESIVE DIS 3M Tape and bandage, adhesive

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FQM Bandage, Elastic General Hospital Class 1 880.5075 2003-06-05
IME Pack, Hot Or Cold, Reusable Physical Medicine Class 1 890.5700 1997-02-20
EZS Appliance, Colostomy, Disposable Gastroenterology, Urology Class 1 876.5900 1996-04-08
KGX Tape And Bandage, Adhesive General Hospital Class 1 880.5240 2003-08-21

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

3M COMPANY
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3005088750 3M POLAND MANUFACTURING SP. Z O.O WROCLAW Dolnoslaskie, PL
3006580861 3M Japan Products Limited Higashine-shi Yamagata, JP
1929938 3M COMPANY Valley, NE, US
2122594 3M COMPANY Hutchinson, MN, US
3008512935 3M Deutschland GmbH Neuss North Rhine-Westphalia, DE

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
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
K870091 Avery Intl. IV SECUREMENT DEVICE USING PCCE THERMO. FILM 1987-02-04

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1717046. Last updated year: 2026. Please use registration number 1717046 when referencing this establishment in official correspondence.
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